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Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
Olfa Hdiji, Emna Turki, Nouha Bouzidi, Imen Bouchhima, Mariem Damak, Saeed Bohlega, Chokri Mhiri
JMD. 2016;9(2):120-123.   Published online 2016 May 25    DOI:

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Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
Journal of Movement Disorders. 2016;9(2):120-123   Crossref logo
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A novel splice site mutation in gene C2orf37 underlying Woodhouse–Sakati syndrome (WSS) in a consanguineous family of Pakistani origin
Gene. 2011;490(1-2):26-31   Crossref logo
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A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome
Clinical Genetics. 2010;78(6):594-597   Crossref logo
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Phenotypic heterogeneity in Woodhouse-Sakati syndrome: Two new families with a mutation in the C2orf37 gene
American Journal of Medical Genetics Part A. 2011;155(11):2647-2653   Crossref logo
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C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
Clinical Genetics. 2010;78(6):585-590   Crossref logo
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Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in theC2orf37Gene
Pediatric Dermatology. 2013;31(1):83-87   Crossref logo
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Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse–Sakati syndrome
Journal of Genetics. 2015;94(3):489-492   Crossref logo
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Woodhouse–Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF 17 gene
Clinical and Experimental Dermatology. 2019;45(2):159-164   Crossref logo
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Japanese siblings with woodhouse-sakati syndrome: The first family in East Asia
Journal of the Neurological Sciences. 2017;381:457   Crossref logo
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Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
Frontiers in Genetics. 2021;12:   Crossref logo

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