RecName: Full=DDB1- and CUL4-associated factor 17

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Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family. [J Clin Lab Anal. 2022]
Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family.
Fozia F, Shah K, Nazli R, Khan SA, Ahmad I, Mohammad N, Khan S, Alotaibi A. J Clin Lab Anal. 2022 Jan; 36(1):e24127. Epub 2021 Dec 8.
Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies. [Saudi Med J. 2021]
Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies.
Alharbi MS. Saudi Med J. 2021 Nov; 42(11):1237-1242.
Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene. [Clin Exp Dermatol. 2020]
Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene.
Shah K, Jan A, Ahmad F, Basit S, Ramzan K, Ahmad W. Clin Exp Dermatol. 2020 Mar; 45(2):159-164. Epub 2019 Aug 28.

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Q5H9S7 [Domain Mapping of Disease Mut...]
Q5H9S7
Domain Mapping of Disease Mutations
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