The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A

Nature Genetics

Volumn 1, Issue 3, 1992, Pages 159-165

  Patel, Pragna I ^a   Roa, Benjamin B ^a   Welcher, Andrew A ^b,c   Schoener Scott, Raymond ^a   Trask, Barbara J ^d   Pentao, Liu ^a   Snipes, G Jackson ^c   Garcia, Carlos A ^e   Francke, Uta ^c   Shooter, Eric M ^c   Lupski, James R ^a   Suter, Ueli ^c  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b AMGEN INC   (United States)

^c STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d LAWRENCE LIVERMORE NATIONAL LABORATORY   (United States)

^e LOUISIANA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

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

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CHROMOSOME 17; CHROMOSOME MAP; CLASSIFICATION; DISEASE MODEL; FEMALE; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MOLECULAR GENETICS; MOUSE; MOUSE MUTANT; MULTIGENE FAMILY; NUCLEOTIDE SEQUENCE; PEDIGREE;

AMINO ACID SEQUENCE; ANIMAL; BASE SEQUENCE; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DISEASE MODELS, ANIMAL; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; HUMAN; MICE; MICE, NEUROLOGIC MUTANTS; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; MYELIN PROTEINS; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026879614     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0692-159     Document Type: Article

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