Prenatal diagnosis in laminin α2 chain (merosin)-deficient congenital muscular dystrophy: A collective experience of five international centers-Reference-Cited by-同舟云学术

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Prenatal diagnosis in laminin α2 chain (merosin)-deficient congenital muscular dystrophy: A collective experience of five international centers

Published:2005-10 Issue:9-10 Volume:15 Page:588-594
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Vainzof Mariz,Richard Pascale,Herrmann Ralf,Jimenez-Mallebrera Cecilia,Talim Beril,Yamamoto Lydia U.,Ledeuil Céline,Mein Rachael,Abbs Stephen,Brockington Martin

Publisher

Elsevier BV

Subject

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

Cited by 32 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. An International Retrospective Early Natural History Study of LAMA2-Related Dystrophies;Journal of Neuromuscular Diseases;2024-08-22

2. Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients;Frontiers in Genetics;2023-06-14

3. Muscular Dystrophies and Allied Disorders III;Muscle Biopsy;2021

4. LAMA2‐related muscular dystrophy: Natural history of a large pediatric cohort;Annals of Clinical and Translational Neurology;2020-09-10

5. LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness;Frontiers in Molecular Neuroscience;2020-08-05

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