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CEP41

centrosomal protein 41

gene with protein productOMIM: 6105232 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in2
Isolated Joubert syndromeORPHA:475
→
Joubert syndrome with ocular defectORPHA:220493
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Данные: Orphadata (CC-BY-4.0)