Author:
Feit Howard,Silbergleit Alice,Schneider Lori B.,Gutierrez Jorge A.,Fitoussi Reine-Paule,Réyès Cécile,Rouleau Guy A.,Brais Bernard,Jackson Charles E.,Beckmann Jacques S.,Seboun Eric
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Newest approaches to diagnosis and pathogenesis of sporadic inclusion-body myositis and hereditary inclusion-body myopathies, including molecular-pathologic similarities to Alzheimer disease;Askanas,1998
2. Inclusion-body myositis and myopathies,1998
3. Limb-girdle muscular dystrophy 1A: refinement of the 5q31 localization and a physical and genetic map of the interval;Bartoloni;Am J Hum Genet Suppl,1997
4. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p;Bashir;Hum Mol Genet,1994
5. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) to chromosome 2p12;Bejaoui;Neurology,1995
Cited by
124 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献