A study on duplications of the dystrophin gene: Evidence of a geographical difference in the distribution of breakpoints by intron

Author:

Galvagni Federico,Saad Fawzy A.,Danieli Gian Antonio,Miorin Marta,Vitiello Libero,Mostacciuolo Maria Luisa,Angelini Corrado

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Beggs AH, Hoffman EP, Snyder JR, Arahata K, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel LM (1991) Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies. Am J Hum Genet 49:54–67

2. Bettecken T, Mueller CR (1991) Direct gene test for Duchenne muscular dystrophy in families without living patients. In: Angelini C, Danieli GA, Fontanari D (eds) Muscular dystrophy research. Excerpta Medica, Amsterdam, pp 77–83

3. Cooke A, Lanyon WG, Wilcox DE, Doman ES, Kataki A, Gillar EF, McWhinnie AIM, Morris A, Ferguson-Smith MA, Connor JM (1990) Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes. J Med Genet 27:292–297

4. Cooper DN, Krawczak M (1993) Human gene mutation. BIOS Scientific Publishers, Oxford, pp 219–224

5. Danieli GA, Mioni F, Mueller CR, Vitiello L, Mostacciuolo ML, Grimm T (1993) Patterns of deletions of the dystrophin gene in different European populations. Hum Genet 91:342–346

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