G.P.40 LGMD2G with clinical presentation of congenital muscular dystrophy: A rare phenotype-Reference-Cited by-同舟云学术

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G.P.40 LGMD2G with clinical presentation of congenital muscular dystrophy: A rare phenotype

Published:2012-10 Issue:9-10 Volume:22 Page:831
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Almeida C.F.,Lima B.L.,Onofre-Oliveira P.C.G.,Pavanello R.C.M.,Zatz M.,Vainzof M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Cited by 8 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. Muscle ultrastructure and histopathological findings in a Brazilian single-centre series of genetically classified telethoninopathy patients;Surgical and Experimental Pathology;2024-08-10

2. Unique Clinical, Radiological and Histopathological Characteristics of a Southeast Asian Cohort of Patients with Limb-Girdle Muscular Dystrophy 2G/LGMD-R7-Telethonin-Related;Journal of Neuromuscular Diseases;2023-01-03

3. Late onset distal myopathy: A new telethoninopathy;Neuromuscular Disorders;2019-01

4. A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature;Neuromuscular Disorders;2018-06

5. Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient;Neuromuscular Disorders;2017-09

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