Two novel mutations (10410 T-->G; 10296 del C) at carboxy-terminus of the dystrophin gene associated with mental retardation. Mutations in brief no. 149. Online.

Human mutation

Volumn 12, Issue 1, 1998, Pages 70-

  Cau, M ^a   Cao, A ^a   Loi, D ^a   Puddu, A ^a   Muntoni, F ^a   Mateddu, A ^a   Melis, M A ^a  

^a UNIVERSITY OF CAGLIARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; PEPTIDE;

ARTICLE; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; HUMAN; ITALY; MENTAL DEFICIENCY; MUTATION;

DYSTROPHIN; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; ITALY; MENTAL RETARDATION; MUTATION; PEPTIDES;

MLCS; MLOWN;

EID: 0032222930     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(1998)12:1<70::aid-humu13>3.0.co;2-g     Document Type: Article

References (0)