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PRR12

proline rich 12

gene with protein productOMIM: 6166331 заболевание
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in1
Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndromeORPHA:659904
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Данные: Orphadata (CC-BY-4.0)