The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication

Nature Genetics

Volumn 1, Issue 3, 1992, Pages 171-175

  Timmerman, V ^a   Nelis, E ^a   Van Hul, W ^a   Nieuwenhuijsen, B W ^b   Chen, K L ^b   Wang, S ^b   Othman, K Ben ^c   Cullen, B ^c   Leach, R J ^d   Hanemann, C O ^e   De Jonghe, P ^a   Raeymaekers, P ^a   van Ommen, G J B ^f   Martin, J J ^a   Muller H W ^e   Vance, J M ^c   Fischbeck, K H ^b   Van Broeckhoven, C ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c DUKE UNIVERSITY MEDICAL CENTER   (United States)

^d UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

^e HEINRICH HEINE UNIVERSITY   (Germany)

^f LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MYELIN PROTEIN; PERIPHERAL MYELIN PROTEIN 22; PERIPHERAL MYELIN PROTEIN-22;

ARTICLE; CHROMOSOME 17; CHROMOSOME MAP; CLASSIFICATION; FEMALE; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOLECULAR GENETICS; MULTIGENE FAMILY; NUCLEOTIDE SEQUENCE; PEDIGREE;

BASE SEQUENCE; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DNA; FEMALE; HUMAN; MALE; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; MYELIN PROTEINS; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026879615     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0692-171     Document Type: Article

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