|
Volumn 26, Issue 3, 2005, Pages 283-
|
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies.
a a a a a a a a a a a a a a a |
Author keywords
[No Author keywords available]
|
Indexed keywords
DYSF PROTEIN, HUMAN;
LIPOCORTIN 1;
LIPOCORTIN 2;
MEMBRANE PROTEIN;
MUSCLE PROTEIN;
ADOLESCENT;
ADULT;
AGED;
ARTICLE;
FEMALE;
GENETICS;
HUMAN;
MALE;
METABOLISM;
MIDDLE AGED;
MUSCULAR DYSTROPHY;
MUTATION;
PHENOTYPE;
PROGNOSIS;
ADOLESCENT;
ADULT;
AGED;
ANNEXIN A1;
ANNEXIN A2;
FEMALE;
HUMANS;
MALE;
MEMBRANE PROTEINS;
MIDDLE AGED;
MUSCLE PROTEINS;
MUSCULAR DYSTROPHIES;
MUTATION;
PHENOTYPE;
PROGNOSIS;
|
EID: 33746701373
PISSN: None
EISSN: 10981004
Source Type: Journal
DOI: 10.1002/humu.9364 Document Type: Article |
Times cited : (67)
|
References (0)
|