Associated Papers
Compound heterozygous WDR19 variants associated with nephronophthisis, Caroli disease, refractory epilepsy and congenital bilateral central blindness: Case report.
Tang X et al.
Heliyon, 2024
Is C1q nephropathy associated with a WDR19 gene mutation? A case report.
Kaynar K et al.
Hippokratia, 0
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