Nanodysferlins support membrane repair and binding to TRIM72/MG53 but do not localize to t-tubules or stabilize Ca2+ signaling-Reference-Cited by-同舟云学术

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Nanodysferlins support membrane repair and binding to TRIM72/MG53 but do not localize to t-tubules or stabilize Ca2+ signaling

Published:2024-06 Issue:2 Volume:32 Page:101257
ISSN:2329-0501
Container-title:Molecular Therapy - Methods & Clinical Development
language:en
Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Muriel Joaquin,Lukyanenko Valeriy,Kwiatkowski Thomas A.^ORCID,Li Yi,Bhattacharya Sayak,Banford Kassidy K.,Garman Daniel,Bulgart Hannah R.,Sutton Roger B.,Weisleder Noah,Bloch Robert J.^ORCID

Funder

Jain Foundation

National Institutes of Health

Publisher

Elsevier BV

Reference70 articles.

1. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families;Passos-Bueno;Med. Genet.,1996

3. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy;Liu;Nat. Genet.,1998

4. Positional cloning of the gene for Miyoshi myopathy and limb-girdle muscular dystrophy;Aoki;Rinsho Shinkeigaku,1999

5. Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy;Illarioshkin;Neurology,2000

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