Very low penetrance in 85 Japanese families with facioscapulohumeral muscular dystrophy 1A-Reference-Cited by-同舟云学术

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Very low penetrance in 85 Japanese families with facioscapulohumeral muscular dystrophy 1A

Published:2004-01-01 Issue:1 Volume:41 Page:12e-12
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Goto K

Publisher

BMJ

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. French National Protocol for diagnosis and care of facioscapulohumeral muscular dystrophy (FSHD);Journal of Neurology;2024-07-02

2. Post-transcriptional RNA stabilization of telomere-proximal RNAs FRG2, DBET, D4Z4 at human 4q35 in response to genotoxic stress and D4Z4 macrosatellite repeat length;2024-03-22

3. Post-transcriptional RNA stabilization of telomere-proximal RNAs FRG2, DBET, D4Z4 at human 4q35 in response to genotoxic stress and D4Z4 macrosatellite repeat length;2024-03-19

4. Case report: Identification of facioscapulohumeral muscular dystrophy 1 in two siblings with normal phenotypic parents using optical genome mapping;Frontiers in Neurology;2024-02-01

5. Thymectomy in myasthenia gravis;Current Opinion in Neurology;2023-07-25

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