Is myotonic dystrophy a single-gene disorder?

Biochemical Society Transactions

Volumn 24, Issue 2, 1996, Pages 510-513

  Johnson, K J ^a,b,c   Boucher, C A ^a,b,c   King, S K ^a,b,c   Winchester, C L ^a,b,c   Bailey, M E S ^a,b,c   Hamilton, G M ^a,b,c   Carey, N ^a,b,c  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

^b Genetics Unit   (United Kingdom)

^c IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; PROTEIN KINASE; TRINUCLEOTIDE;

ALOPECIA; AMINO ACID SEQUENCE; CATARACT; CLINICAL FEATURE; CONFERENCE PAPER; EXON; GENETIC DISORDER; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; HUMAN CELL; INTRON; MENTAL DEFICIENCY; MUSCLE ATROPHY; MUSCLE HYPOTONIA; MYOTONIA; MYOTONIC DYSTROPHY; PHENOTYPE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING; STOP CODON;

EID: 0029993053     PISSN: 03005127     EISSN: None     Source Type: Journal    
DOI: 10.1042/bst0240510     Document Type: Conference Paper

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