Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: Possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis

Biochemical and Biophysical Research Communications

Volumn 268, Issue 2, 2000, Pages 612-616

  Awata, Takuya ^a   Inoue, Kiyoaki ^a   Kurihara, Susumu ^a   Ohkubo, Tomoko ^a   Inoue, Ikuo ^a   Abe, Takahiro ^b   Takino, Hirofumi ^b   Kanazawa, Yasunori ^c   Katayama, Shigehiro ^a  

^a SAITAMA MEDICAL UNIVERSITY   (Japan)

^b NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c JICHI MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; AUTOANTIBODY; HISTIDINE; MEMBRANE PROTEIN; PANCREAS ISLET CELL ANTIBODY;

ADOLESCENT; ADULT; AGED; ALLELE; ARTICLE; AUTOIMMUNE DISEASE; CELL SURVIVAL; CHILD; CONTROLLED STUDY; DIABETES INSIPIDUS; GENE FREQUENCY; GENE FUNCTION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; HASHIMOTO DISEASE; HEARING IMPAIRMENT; HUMAN; HUMAN TISSUE; INSULIN DEPENDENT DIABETES MELLITUS; JAPAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; OPTIC NERVE ATROPHY; PANCREAS ISLET BETA CELL; POPULATION RESEARCH; PRIORITY JOURNAL; WOLFRAM SYNDROME;

EID: 0034673246     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2000.2169     Document Type: Article

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