Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples-Reference-Cited by-同舟云学术

Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples

Published:2015-06-03 Issue:1 Volume:53 Page:44-48
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Straathof Chiara S.M.¹,Van Heusden Dave²,Ippel Pieternella F.³,Post Jan G.³,Voermans Nicol C.⁴,De Visser Marianne⁵,Brusse Esther⁶,Van Den Bergen Janneke C.¹,Van Der Kooi Anneke J.⁵,Verschuuren Jan J.G.M.¹,Ginjaar Hendrika B.²

Affiliation:

1. Department of Neurology; Leiden University Medical Center; P.O. Box 9600 2300RC Leiden The Netherlands

2. Department of Clinical Genetics; Leiden University Medical Center; Leiden The Netherlands

3. Department of Medical Genetics; University Medical Center Utrecht; Utrecht The Netherlands

4. Department of Neurology; Radboud University Medical Center; Nijmegen The Netherlands

5. Department of Neurology, Academic Medical Center; University of Amsterdam; Amsterdam The Netherlands

6. Department of Neurology; Erasmus MC University Medical Center; Rotterdam The Netherlands

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.24691/fullpdf

Reference25 articles.

1. A new X-chromosomal muscular dystrophy;Becker;Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr,1955

2. A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers;Rotthauwe;Humangenetik,1966

3. Becker-type muscular dystrophy;Bradley;Muscle Nerve,1978

4. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities;Bushby;J Neurol,1993

5. Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene;Gospe;Neurology,1989

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