Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis.

Human mutation

Volumn 26, Issue 1, 2005, Pages 59-

  White, Stefan J ^a   Uitte de Willige, Shirley ^a   Verbove, Dennis ^a   Politano, Luisa ^a   Ginjaar, Ieke ^a   Breuning, Martijn H ^a   den Dunnen, Johan T ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

SARCOGLYCAN;

ALLELE; ARTICLE; CONSANGUINITY; EXON; FEMALE; GENE DELETION; GENETIC SCREENING; GENETICS; HAPLOTYPE; HUMAN; MALE; MOLECULAR GENETICS; MUSCULAR DYSTROPHY; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; POLYMERASE CHAIN REACTION;

ALLELES; BASE SEQUENCE; CONSANGUINITY; EXONS; FEMALE; GENETIC SCREENING; HAPLOTYPES; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHIES; PEDIGREE; POLYMERASE CHAIN REACTION; SARCOGLYCANS; SEQUENCE DELETION;

EID: 33748579267     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9347     Document Type: Article

References (0)