Molecular and cellular basis of genetically inherited skeletal muscle disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology
Link
https://www.nature.com/articles/s41580-021-00389-z.pdf
Reference268 articles.
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3. Monaco, A. P., Bertelson, C. J., Colletti-Feener, C. & Kunkel, L. M. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy. Hum. Genet. 75, 221–227 (1987).
4. Hoffman, E. P., Brown, R. H. & Kunkel, L. M. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51, 919–928 (1987). First description of the dystrophin protein, which is encoded by DMD, the causal gene underlying DMD.
5. Gittings, L. M. & Sattler, R. Recent advances in understanding amyotrophic lateral sclerosis and emerging therapies. Fac. Rev. 9, 12 (2020).
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