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has major subject area list
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Deafness; Diabetes Mellitus, Type 2; Insulin; Point Mutation; RNA, Transfer, Leu
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has minor subject area list
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Adenine; Adolescent; Adult; Aged; Arginine; Blood Glucose; Body Mass Index; C-Peptide; Child; Child, Preschool; Female; Genomic Imprinting; Glucose Tolerance Test; Glycated Hemoglobin; Guanine; Humans; Insulin Secretion; Male; Middle Aged; Pedigree; Periodicity; Phenotype; Reference Values; Sex Characteristics
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information resource reference
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Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation. Diabetes. 1996 Apr; 45(4):478-87.
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label
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Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
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