Author:
Beckmann J.S,Brown R.H,Muntoni F,Urtizberea A,Bonnemann C,Bushby K.M.D
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
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4. Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localisation to 5q31;Feit;Am J Hum Genet,1998
5. Genetic localisation of a newly recognised autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21;van der Kooi;Am J Hum Genet,1997
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