Oculopharyngeal Muscular Dystrophy Associated with Dementia-Reference-Cited by-同舟云学术

Oculopharyngeal Muscular Dystrophy Associated with Dementia

Published:2011 Issue:20 Volume:50 Page:2409-2412
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Mizoi Yoshikazu¹,Yamamoto Toshimasa¹,Minami Narihiro²,Ohkuma Aya¹,Nonaka Ikuya²,Nishino Ichizo²,Tamura Naotoshi¹,Amano Takahiro³,Araki Nobuo¹

Affiliation:

1. Department of Neurology, Faculty of Medicine, Saitama Medical University, Japan

2. National Institute of Neuroscience, National Center of Neurology and Psychiatry, Japan

3. Department of Medical Educational Center, Faculty of Medicine, Keio University, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

http://www.jstage.jst.go.jp/article/internalmedicine/50/20/50_20_2409/_pdf

Reference15 articles.

1. 1. Brais B, Tome E. Oculopharyngeal muscular dystrophy. In: Myology. Engel A, Laurea C, Eds. McGraw-Hill, New York, 2004: 1147-1162.

2. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

3. 3. Brais B, Xie YG, Sanson M, et al. The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain gene on chromosome 14q 11.2-q13. Hum Mol Genet 4: 429-434, 1995.

4. 4. Brais B, Rouleau G. Oculopharyngeal Muscular Dystrophy. Gene Reviews, Pagon RA, Bird TD, Dolan CR, Stephens K, Eds. 2006 http://www.genetests.org

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