Intragenic deletion patterns of dystrophin gene in Duchenne and Becker muscular dystrophy patients from Algeria-Reference-Cited by-同舟云学术

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Intragenic deletion patterns of dystrophin gene in Duchenne and Becker muscular dystrophy patients from Algeria

Published:2013-08-14 Issue:1 Volume:36 Page:17-24
ISSN:1976-9571
Container-title:Genes & Genomics
language:en
Short-container-title:Genes Genom

Author:

Cherrallah Amira,Benhassine Traki,Nouioua Sonia,Makri Samira,Chaouch Malika,Tazir Meriem,Hamadouche Tarik

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s13258-013-0134-0.pdf

Reference40 articles.

1. Aartsma-Rus A, Van Deutekom JCT, Fokkema IF, Van Ommen GJB, Den Dunnen JT (2006) Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule. Muscle Nerve 34:135–144

2. Aartsma-Rus A, Fokkema I, Verschuuren J, Ginjaar I, van Deutekom J, van Ommen GJ, den Dunnen JT (2009) Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations. Hum Mutat 30:293–299

3. Azibi K, Bachner L, Beckmann JS, Matsumura K, Hamouda E, Chaouch M, Chaouch A, Ait-Ouarab R, Vignal A, Weissenbach J, Vinet MC, Letrucq F, Collin H, Tome FMS, Reghis A, Fardeau M, Campbell KP, Kaplan JC (1993) Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12. Hum Mol Genet 2:1423–1428

4. Baranov VS, Gorbunova VN, Malysheva OV, Artemyeva OV, Kascheeva TK, Evgrafov OV, Polyakov AV, Lebedev VM, Kuznetzova TV, Shlykova SN, Mikhailov AV, Vakharlovsky VG (1993) Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia. Prenat Diagn 13:323–333

5. Beggs AH, Koenig M, Boyce FM, Kunkel LM (1990) Detection of 98 % of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet 86:45–48

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