Small Mutations of the DMD Gene in Taiwanese Families
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference23 articles.
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2. Dystrophin. The gene and its product;Mandel;Nature,1989
3. 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
4. Dystrophin and mutations: one gene, several proteins, multiple phenotypes;Muntoni;Lancet Neurol,2003
5. Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule;Aartsma-Rus;Muscle Nerve,2006
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2. Cost-Effectiveness Analysis of Diagnosis of Duchenne/Becker Muscular Dystrophy in Colombia;Value in Health Regional Issues;2018-12
3. The natural history of the patients with Duchenne muscular dystrophy in Taiwan: A medical center experience;Pediatrics & Neonatology;2018-04
4. Novel mutation in exon 56 of the dystrophin gene in a child with Duchenne muscular dystrophy;International Journal of Molecular Medicine;2013-09-18
5. Genetic Analysis of Dystrophin Gene for Affected Male and Female Carriers with Duchenne/Becker Muscular Dystrophy in Korea;Journal of Korean Medical Science;2012
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