The KMDB/MutationView: A mutation database for human disease genes

Nucleic Acids Research

Volumn 29, Issue 1, 2001, Pages 327-328

  Minoshima, Shinsei ^a   Mitsuyama, Susumu ^a   Ohtsubo, Masafumi ^a   Kawamura, Takashi ^a   Ito, Sachiko ^b   Shibamoto, Sayumi ^b   Ito, Fumiaki ^b   Shimizu, Nobuyoshi ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b SETSUNAN UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOIMMUNITY; BLOOD DISEASE; BRAIN DISEASE; CANCER; COMPUTER PROGRAM; DATA BASE; EAR DISEASE; EYE DISEASE; GENE MUTATION; GENETIC DISORDER; HEART DISEASE; HUMAN; IMMUNOPATHOLOGY; INTERNET; MUSCLE DISEASE; PRIORITY JOURNAL; SYNDROME;

EID: 0035175740     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/29.1.327     Document Type: Article

References (3)

1. Keio Mutation Database (KMDB) for human disease gene mutations
2. Deletion mutation in a novel ubiquitin-like protein (PARKIN) gene causes autosomal recessive juvenile Parkinsonism (AR-JP)
3. Cystic fibrosis