Four novel mutations associated with autosomal recessive inclusion body myopathy (MIM: 600737)
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference22 articles.
1. An Italian family with autosomal recessive quadriceps-sparing inclusion body myopathy (ARQS-JBM) linked to chromosome 9p1;Mirabella;Neurol. Sci.,2000
2. Various types of hereditary inclusion body myopathies map to chromosome 9p1–q1;Argov;Ann. Neurol.,1997
3. “Rimmed vacuole myopathy” sparing the quadriceps: a unique disorder in Iranian Jews;Argov;J. Neurol. Sci.,1984
4. Sporadic inclusion body-myositis and hereditary inclusion-body myopathies;Askanas;Arch. Neurol.,1998
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