Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection-Reference-Cited by-同舟云学术

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Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection

Published:2008-06-28 Issue:6 Volume:39 Page:419-424
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Asano Jun-Ichi,Tomatsu Shunji,Sukegawa Kazuko,Ikedo Yuko,Minami Ryoji,Iida Mitsuo,Nishimura Masaaki,Nakagawa Masanori,Ohshiro Morio,Orii Tadao

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03052.x/fullpdf

Reference11 articles.

1. Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies;Baumbach;Neurology,1989

2. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies;Forrest;Genomics,1988

3. Molecular deletions in the Duchenne/Becker muscular dystrophy gene;Hart;Clin. Genet.,1989

4. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig;Cell,1987

5. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion;Koenig;Am. J. Hum. Genet.,1989

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. Espectro mutacional de la distrofia muscular de Duchenne en España: estudio de 284 casos;Neurología;2017-07

2. Mutational spectrum of Duchenne muscular dystrophy in Spain: study of 284 cases;Neurología (English Edition);2017-07

3. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families – Detection of carrier status in symptomatic and asymptomatic female relatives;Neuromuscular Disorders;2009-02

4. Carrier Diagnosis of Duchenne Muscular Dystrophy Using Fluorescent CA Repeat Polymorphism;Congenital Anomalies;2008-06-28

5. Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: The use of new designed primers for the analysis of the major deletion “hot spot” region;American Journal of Medical Genetics;1997-06-13

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