The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
Richard, I., Broux, O., Allamand, V., Fougerousse, F., Chiannilkulchai, N., Bourg, N., Brenguier, L., Devaud, C., Pasturaud, P., Roudaut, C., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90368-2 · Cited by 1,001
Self-citationThree muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage
Campbell, K. P. (1995) · Cell · doi:10.1016/0092-8674(95)90344-5 · Cited by 829
(1965) · Medical Journal of Australia · doi:10.5694/j.1326-5377.1965.tb71746.x · Cited by 585
Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy
Noguchi, S., McNally, E. M., Othmane, K. B., Hagiwara, Y., Mizuno, Y., Yoshida, M., Yamamoto, H., Bönnemann, C. G., Gussoni, E., Denton, P. H., et al. (1995) · Science · doi:10.1126/science.270.5237.819 · Cited by 506
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
Roberds, S. L., Leturcq, F., Allamand, V., Piccolo, F., Jeanpierre, M., Anderson, R. D., Lim, L. E., Lee, J. C., Tomé, F. M. S., Romero, N. B., et al. (1994) · Cell · doi:10.1016/0092-8674(94)90527-4 · Cited by 454
β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12
Lim, L. E., Duclos, F., Broux, O., Bourg, N., Sunada, Y., Allamand, V., Meyer, J., Richard, I., Moomaw, C., Slaughter, C., et al. (1995) · Nature Genetics · doi:10.1038/ng1195-257 · Cited by 447
Bönnemann, C. G., Modi, R., Noguchi, S., Mizuno, Y., Yoshida, M., Gussoni, E., McNally, E. M., Duggan, D. J., Angelini, C., Hoffman, E. P., et al. (1995) · Nature Genetics · doi:10.1038/ng1195-266 · Cited by 445
Dystrophin-associated proteins in muscular dystrophy
Ozawa, E., Yoshida, M., Suzuki, A., Mizuno, Y., Hagiwara, Y., & Noguchi, S. (1995) · Human Molecular Genetics · doi:10.1093/hmg/4.suppl_1.1711 · Cited by 242
Ibraghimov‐Beskrovnaya, O., Milatovich, A., Özçelık, T., Yang, B., Koepnick, K., Francke, U., & Campbell, K. P. (1993) · Human Molecular Genetics · doi:10.1093/hmg/2.10.1651 · Cited by 230
Yoshida, M., Suzuki, A., Yamamoto, H., Noguchi, S., Mizuno, Y., & Ozawa, E. (1994) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1994.tb18958.x · Cited by 212
Cited by
Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies
Michele, D. E., Barresi, R., Kanagawa, M., Saito, F., Cohn, R. D., Satz, J. S., Dollar, J., Nishino, I., Kelley, R. I., Somer, H., et al. (2002) · Nature · doi:10.1038/nature00837 · Cited by 779
Bashir, R., Britton, S., Strachan, T., Keers, S., Vafiadaki, E., Lako, M., Richard, I., Marchand, S., Bourg, N., Argov, Z., et al. (1998) · Nature Genetics · doi:10.1038/1689 · Cited by 688
Self-citationMuchir, A. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.9.1453 · Cited by 616
Durbeej, M., & Campbell, K. P. (2002) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(02)00309-x · Cited by 435
Weiler, T., Greenberg, C. R., Zelinski, T., Nylen, E., Coghlan, G., Crumley, M. J., Fujiwara, T. M., Morgan, K., & Wrogemann, K. (1998) · The American Journal of Human Genetics · doi:10.1086/301925 · Cited by 115
Metadata
- Authors
- Nigro, V., Moreira, E. D. S., Piluso, G., Vainzof, M., Belsito, A., Politano, L., Puca, A. A., Passos-Bueno, M. R., & Zatz, M.
- Venue
- Nature Genetics
- Published
- 1996-10
- Volume
- 14
- Issue
- 2
- Pages
- 195-198
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2320022870
- Cited by
- 423
- References
- 22
- FWCI
- 11.63
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene. https://app.cochat.ai/papers/10.1038/ng1096-195
- The paper
- Nigro, V., Moreira, E. D. S., Piluso, G., Vainzof, M., Belsito, A., Politano, L., Puca, A. A., Passos-Bueno, M. R., & Zatz, M. (1996). Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene. Nature Genetics. https://doi.org/10.1038/ng1096-195
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
