High frequency of mutations in codon 98 of the peripheral myelin protein Po gene in 20 French CMT1 patients [3]

American Journal of Human Genetics

Volumn 58, Issue 3, 1996, Pages 638-641

  Rouger, H ^a   LeGuern, E ^a   Gouider, R ^a   Tardieu, S ^a   Birouk, N ^a   Gugenheim, M ^a   Bouche, P ^a   Agid, Y ^a   Brice, A ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN;

CLINICAL ARTICLE; CODON; FAMILY HISTORY; GENE DUPLICATION; GENE FREQUENCY; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; LETTER; PRIORITY JOURNAL; PROTEIN ISOLATION; RESTRICTION MAPPING;

BASE SEQUENCE; CHARCOT-MARIE-TOOTH DISEASE; CODON; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MYELIN P0 PROTEIN; PEDIGREE;

EID: 0030051641     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)