Oculopharyngeal muscular dystrophy with PABPN1 mutation in a Chinese Malaysian woman-Reference-Cited by-同舟云学术

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Oculopharyngeal muscular dystrophy with PABPN1 mutation in a Chinese Malaysian woman

Published:2005-03 Issue:3 Volume:15 Page:262-264
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Goh Khean Jin,Wong Kum Thong,Nishino Ichizo,Minami Narihiro,Nonaka Ikuya

Publisher

Elsevier BV

Subject

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

Reference13 articles.

1. Oculopharyngeal muscular dystrophy;Victor;N Engl J Med,1962

2. Oculopharyngeal muscular dystrophy;Brais;Semin Neurol,1999

3. expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat Genet,1998

4. Epidemiology and inheritance of oculopharyngeal muscular dystrophy in Israel;Blumen;Neuromuscular Disord,1997

Cited by 9 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. A Japanese case of oculopharyngeal muscular dystrophy (OPMD) with PABPN1 c.35G > C; p.Gly12Ala point mutation;BMC Neurology;2021-07-05

2. Recent Progress in Oculopharyngeal Muscular Dystrophy;Journal of Clinical Medicine;2021-03-29

3. Oculopharyngeal Muscular Dystrophy, an Often Misdiagnosed Neuromuscular Disorder: A Southern California Experience;Journal of Clinical Neuromuscular Disease;2019-12

4. Oculopharyngeal Muscular Dystrophy in Singapore: Not So Rare;Annals of the Academy of Medicine, Singapore;2018-08-15

5. Oculopharyngeal Muscular Dystrophy: Phenotypic and Genotypic Studies in a Chinese Population;NeuroMolecular Medicine;2014-10-05

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