Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients (Q47306165)

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scientific article published in October 2004
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Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients
scientific article published in October 2004

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    Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients (English)

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