Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families.

Archives de l'Institut Pasteur de Tunis

Volumn 83, Issue 1-4, 2006, Pages 19-23

  Louhichi, N ^a   Richard, P ^a   Triki, C H ^a   Meziou, M ^a   Ayadi, H ^a   Guicheney, P ^a   Fakhfakh, F ^a  

^a UNIVERSITY OF SFAX   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

LAMININ; LAMININ ALPHA2;

ARTICLE; BIOPSY; CASE REPORT; CHILD; CHROMOSOME MAP; CONSANGUINITY; GENETICS; HAPLOTYPE; HUMAN; IMMUNOBLOTTING; MUSCULAR DYSTROPHY; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; RECESSIVE GENE; RESTRICTION MAPPING; TUNISIA;

BIOPSY; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; GENES, RECESSIVE; HAPLOTYPES; HUMANS; IMMUNOBLOTTING; LAMININ; MUSCULAR DYSTROPHIES; MUTATION; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; RESTRICTION MAPPING; TUNISIA;

EID: 66349126277     PISSN: 00202509     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)