Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy

American Journal of Human Genetics

Volumn 52, Issue 6, 1993, Pages 1164-1174

  Harley, H G ^a   Rundle, S A ^a   MacMillan, J C ^a   Myring, J ^a   Brook, J D ^a   Crow, S ^a   Reardon, W ^a   Fenton, I ^a   Shaw, D J ^a   Harper, P S ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CATARACT; CLINICAL FEATURE; GENE MUTATION; HUMAN; MYOTONIA; MYOTONIC DYSTROPHY; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGING; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; HUMAN; INFANT; INFANT, NEWBORN; MALE; MIDDLE AGE; MYOTONIC DYSTROPHY; PARENTS; PHENOTYPE; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0027485748     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)