Maternally Inherited Diabetes and Deafness (MIDD) Syndrome: A Clinical and Molecular Genetic Study of a Taiwanese Family

Chang Gung Medical Journal

Volumn 27, Issue 1, 2004, Pages 66-73

  Chen, Yung Nien ^a   Liou, Chia Wei ^a,b   Huang, Chin Chang ^b   Lin, Tsu Kung ^a   Wei, Yau Huei ^c  

^a CHANG GUNG UNIVERSITY   (Taiwan)

^b CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

^c NATIONAL YANG MING UNIVERSITY   (Taiwan)

Author keywords

A3243G mutation; Deafness; Diabetes mellitus; Family survey; Mitochondrial DNA

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; CASE REPORT; DIABETES MELLITUS; EVOKED BRAIN STEM AUDITORY RESPONSE; FEMALE; GENE MUTATION; GENETIC DISORDER; HEARING IMPAIRMENT; HEARING TEST; HUMAN; MATERNALLY INHERITED DIABETES AND DEAFNESS SYNDROME; MITOCHONDRION; ORAL GLUCOSE TOLERANCE TEST; PEDIGREE ANALYSIS; SYNDROME DELINEATION;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; DEAFNESS; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; FEMALE; HUMANS; MALE; MIDDLE AGED; POINT MUTATION; SYNDROME; TAIWAN;

EID: 1642324248     PISSN: 02558270     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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