Mutation analysis in charcot-marie-tooth disease type 1 (CMT1)

Human Mutation

Volumn 11, Issue SUPPL 1, 1998, Pages

  Sorour, E ^a   Upadhyaya, M ^a  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

Charcot Marie Tooth disease; Connexin 32 gene (Cx32)IN; Myelin protein zero gene (MPZ); Peripheral myelin protein 22 gene (PMP22)

Indexed keywords

ARTICLE; GENE DUPLICATION; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MUSCLE WEAKNESS; POINT MUTATION; PRIORITY JOURNAL; REMYELINIZATION; AMINO ACID SUBSTITUTION; CHEMISTRY; FEMALE; FRAMESHIFT MUTATION; GENETICS; HETERODUPLEX ANALYSIS; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; SINGLE STRAND CONFORMATION POLYMORPHISM;

CONNEXIN 32; DNA; GAP JUNCTION PROTEIN; MYELIN PROTEIN; PMP22 PROTEIN, HUMAN;

AMINO ACID SUBSTITUTION; CHARCOT-MARIE-TOOTH DISEASE; CONNEXINS; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; FRAMESHIFT MUTATION; HETERODUPLEX ANALYSIS; HUMANS; MALE; MUTATION, MISSENSE; MYELIN P0 PROTEIN; MYELIN PROTEINS; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0031985213     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1380110178     Document Type: Article

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