A family with X-linked dominant Charcot-Marie-Tooth caused by a connexin32 mutation

European Journal of Paediatric Neurology

Volumn 4, Issue 5, 2000, Pages 235-238

  Verhelst, Helene E ^a   Lofgren, Ann ^b   Van Coster, Rudy N ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

Author keywords

Axonal neuropathy; CMTX; Connexin32

Indexed keywords

CONNEXIN 32; DNA; HISTIDINE; TYROSINE;

ARTICLE; CASE REPORT; CHILD; CODON; FAMILY; GENE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; X CHROMOSOME; X CHROMOSOME DOMINANT INHERITANCE;

EID: 0033864281     PISSN: 10903798     EISSN: None     Source Type: Journal    
DOI: 10.1053/ejpn.2000.0311     Document Type: Article

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