Novel mutation of the myelin P0 gene in a CMT1B family

Human Mutation

Volumn 9, Issue 1, 1997, Pages 74-77

  Sorour, E ^a   MacMillan, J ^a   Upadhyaya, M ^a  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MYELIN PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; DEMYELINATING DISEASE; DNA SEQUENCE; FAMILY STUDY; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MALE; PEDIGREE ANALYSIS; PERIPHERAL NEUROPATHY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

ARGININE; CHARCOT-MARIE-TOOTH DISEASE; FEMALE; GENES, DOMINANT; HISTIDINE; HUMANS; MALE; MUTATION; MYELIN PROTEINS; PEDIGREE;

EID: 0031012205     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1997)9:1<74::AID-HUMU16>3.0.CO;2-M     Document Type: Article

References (7)

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