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Samira Ait-El-Mkadem

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Corrigendum: A novel CISD2 mutation associated with a classical wolfram syndrome phenotype alters Ca21 homeostasis and ER-mitochondria interactions. [Human Molecular Genetics (2017)], doi: 10.1093/hmg/ddx060

2017 Human Molecular Genetics
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Association of insulin receptor genetic variants with polycystic ovary syndrome in a population of women from Central Europe

2010 Fertility and Sterility
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Citations (13)