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Cited by 329

The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

Carlton, Victoria E. H., Harris, Baruch Z., Puffenberger, Erik G., Batta, A. K., Knisely, A. S., Robinson, Donna L., Strauss, Kevin A., Shneider, Benjamin L., Lim, Wendell A., Salen, Gerald, Morton, D. Holmes, Bull, Laura N.·2003·Nature Genetics
DOI 10.1038/ng1147
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Registry

Crossref · 10.1038/ng1147

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Metadata

Authors
Carlton, V. E. H., Harris, B. Z., Puffenberger, E. G., Batta, A. K., Knisely, A. S., Robinson, D. L., Strauss, K. A., Shneider, B. L., Lim, W. A., Salen, G., Morton, D. H., & Bull, L. N.
Venue
Nature Genetics
Publisher
Springer Science and Business Media LLC
Published
2003-04-21
Volume
34
Issue
1
Pages
91-96
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
DOI
10.1038/ng1147
OpenAlex
W2027562091
Cited by
329
References
22
FWCI
5.12
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. https://app.cochat.ai/papers/10.1038/ng1147
The paper
Carlton, V. E. H., Harris, B. Z., Puffenberger, E. G., Batta, A. K., Knisely, A. S., Robinson, D. L., Strauss, K. A., Shneider, B. L., Lim, W. A., Salen, G., Morton, D. H., & Bull, L. N. (2003). Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. Nature Genetics. https://doi.org/10.1038/ng1147

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.