A scapular onset muscular dystrophy without facial involvement: Possible allelism with facioscapulohumeral muscular dystrophy

Author:

Jardine P.E.,Upadhyaya M.,Maynard J.,Harper P.,Lunt P.W.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q;Speer;Am J Hum Genet,1992

2. Scapuloperoneal myopathies, myelopathies and neuropathies;Serratrice,1979

3. Adult onset scapuloperoneal myopathy;Thomas;J Neurol Neurosurg Psychiatry,1975

4. Genetic counselling in facioscapulohumeral muscular dystrophy;Lunt;J Med Genet,1991

5. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4;Wijmenga;Lancet,1990

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