Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation (Q34375619)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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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Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation (English)
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Froguel P
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Clément K
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Velho G
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Byrne MM
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Sturis J
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Pueyo ME
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Blanché H
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Vionnet N
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Fiet J
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Passa P
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Robert JJ
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Polonsky KS
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1 April 1996
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45
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478-487
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