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Cited by 303

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Molecular Basis of Genetic Instability of Triplet Repeats

Open access
Wells, Robert D.·1996·Journal of Biological Chemistry

Abstract

A veritable explosion is taking place in our understanding of the human genetics, biochemistry, and DNA structural issues related to human hereditary neuromuscular and neurodegenerative diseases. Also, the non-Mendelian expansion process that elicits these disease manifestations (anticipation) is under intense investigation. Within the last 3 years, the molecular basis of 10 human genetic disorders (including fragile X syndrome (FRAXA and FRAXE), myotonic dystrophy (DM), (1) Kennedy's disease, Huntington's disease (HD), spinocerebellar ataxia type 1 (SCA1), and dentatorubral-pallidoluysian atrophy (DRPLA)) has been partially established (reviewed in (1, 2, 3, 4, 5)).

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Crossref · 10.1074/jbc.271.6.2875

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Metadata

Authors
Wells, R. D.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1996-02
Volume
271
Issue
6
Pages
2875-2878
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2095344231
Cited by
303
References
3
FWCI
13.72
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Molecular Basis of Genetic Instability of Triplet Repeats. https://app.cochat.ai/papers/10.1074/jbc.271.6.2875
The paper
Wells, R. D. (1996). Molecular Basis of Genetic Instability of Triplet Repeats. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.271.6.2875

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.