Heteroplasmic mitochondrial DNA 3310 mutation in NADH dehydrogenase subunit 1 associated with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation in a single patient

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Veröffentlicht in:	Diabetes care 2003-03, Vol.26 (3), p.952-953
Hauptverfasser:	Hattori, Yukiko, Nakajima, Kazuo, Eizawa, Takayuki, Ehara, Takashi, Koyama, Masamichi, Hirai, Tetsuya, Fukuda, Youji, Kinoshita, Moritoshi
Format:	Artikel
Sprache:	eng
Schlagworte:	Cardiomyopathy, Hypertrophic - complications Cardiomyopathy, Hypertrophic - genetics Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - genetics DNA, Mitochondrial - genetics Electron Transport Complex I Humans Intellectual Disability - complications Intellectual Disability - genetics Male Middle Aged NADH, NADPH Oxidoreductases - genetics Point Mutation
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