A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy
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| Description | scientific article |
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author: Hassen Kamoun Faiza Fakhfakh |
| Publication date | February 19, 2015 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |