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Article

DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.

Clinical genetics - 1 Jul 2005

Hamed Sa, Sutherland-Smith Aj, Gorospe Jrm, Kendrick-Jones J, Hoffman Ep

Abstract excerpt

We systematically screened the whole coding region of 18 male muscular dystrophy patients whose clinical, histological and laboratory findings suggest Becker muscular dystrophy (present but abnormal dystrophin). No systematic mutation study of a cohort of patients with dystrophin of normal quality but abnormal quantity has been published. The complete coding sequence of the dystrophin gene (11 kb) of each patient...

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Identifiers

PMID: 15952989
DOI: 10.1111/j.1399-0004.2005.00455.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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