New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

Journal: Neurogenetics

Volume: 

Issue: 

Year of Publication: 2004

Affiliated Institutions: 

Statistics

Citations :  2
Authors :  0

Identifiers

Doi : 10.1007/s10048-003-0165-9
SSN : 

Study Population

Male,Female

Mesh Terms

Other Terms

Study Design

Study Approach

Country of Study

Mali

Publication Country