Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation

被引:5
|
作者
Arai, M [1 ]
Ohshima, S [1 ]
机构
[1] SEIREI MIKATABARA HOSP, DEPT INTERNAL MED, HAMAMATSU, SHIZUOKA 433, JAPAN
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D O I
10.1007/s004150050126
中图分类号
R74 [神经病学与精神病学];
学科分类号
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页码:468 / 469
页数:2
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