Intragenic deletion ofTRIM32in compound heterozygotes with sarcotubular myopathy/LGMD2H-Reference-Cited by-同舟云学术

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Intragenic deletion ofTRIM32in compound heterozygotes with sarcotubular myopathy/LGMD2H

Published:2009-09 Issue:9 Volume:30 Page:E831-E844
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Borg Kristian,Stucka Rolf,Locke Matthew,Melin Eva,Ãhlberg Gabrielle,Klutzny Ursula,Hagen Maja von der,Huebner Angela,LochmÃ¼ller Hanns,Wrogemann Klaus,Thornell Lars-Eric,Blake Derek J.,Schoser Benedikt

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 35 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy;Frontiers in Neurology;2024-01-18

2. Tripartite Motif-Containing Protein 32 (TRIM32): What Does It Do for Skeletal Muscle?;Cells;2023-08-19

3. Autosomal Recessive Limb-Girdle Muscular Dystrophies;Current Clinical Neurology;2023

4. Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation;Neuromuscular Disorders;2021-09

5. TRIM-NHL as RNA Binding Ubiquitin E3 Ligase (RBUL): Implication in development and disease pathogenesis;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2021-07

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