Found: 6
Select item for more details and to access through your institution.
Prevalence of GNE p.M712T and hereditary inclusion body myopathy (HIBM) in Sangesar population of Northern Iran.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 6, p. 589, doi. 10.1111/cge.12086
- By:
- Publication type:
- Article
Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?
- Published in:
- Clinical Genetics, 2011, v. 80, n. 4, p. 398, doi. 10.1111/j.1399-0004.2010.01620.x
- By:
- Publication type:
- Article
C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy.
- Published in:
- 2007
- By:
- Publication type:
- journal article
CAPN3 mutations in patients with idiopathic eosinophilic myositis.
- Published in:
- 2006
- By:
- Publication type:
- Journal Article
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP).
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 291, doi. 10.1034/j.1399-0004.2000.580407.x
- By:
- Publication type:
- Article
Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain).
- Published in:
- Brain: A Journal of Neurology, 1998, v. 121, n. 9, p. 1735, doi. 10.1093/brain/121.9.1735
- By:
- Publication type:
- Article