All individuals with variants in gene NEUROG3

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00451661 3bINP-047 PubMed: Vela-Amieva 2024 Parents with inbreeding and consanguinity (not molecularly tested). Co-occurrence of two different monogenic diseases F yes Mexico Mexican - - - - DIAR4 Growth delay, Type 1 diabetes. Cataract, Intellectual disability, Hepatomegaly. Co-ocurrence with Wagner syndrome 1 (OMIM: 143200) 1 1 Miriam Erandi Reyna-Fabián
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