1 Medica I., "Woodhouse-Sakati syndrome : case report and symptoms review" 18 : 227-231, 2007
2 Gül D., "Wood-house and Sakati syndrome (MIM. 241080): report of a new patient" 9 : 123-125, 2000
3 Koshy G., "Three siblings with Woodhouse-Sakati syndrome in an In-dian family" 17 : 57-60, 2008
4 Ben-Omran T., "Phenotypic heterogeneity in Wood-house-Sakati syndrome: two new families with a mutation in the C2orf37 gene" 155A : 2647-2653, 2011
5 Hogarth P, "Neurodegeneration with brain iron accumula-tion : diagnosis and management" 8 : 1-13, 2015
6 Alazami AM., "Mutations in C2orf37, encoding a nucle-olar protein, cause hypogonadism, alopecia, diabetes mel-litus, mental retardation, and extrapyramidal syndrome" 83 : 684-691, 2008
7 Nanda A., "Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome : report of a family with mutation in the C2orf37 gene" 31 : 83-87, 2014
8 Woodhouse NJ., "A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities" 20 : 216-219, 1983
9 Habib R., "A novel splice site mutation in gene C2orf37 underlying Wood-house-Sakati syndrome(WSS)in a consanguineous family of Pakistani origin" 490 : 26-31, 2011
10 Steindl K., "A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome" 78 : 594-597, 2010
1 Medica I., "Woodhouse-Sakati syndrome : case report and symptoms review" 18 : 227-231, 2007
2 Gül D., "Wood-house and Sakati syndrome (MIM. 241080): report of a new patient" 9 : 123-125, 2000
3 Koshy G., "Three siblings with Woodhouse-Sakati syndrome in an In-dian family" 17 : 57-60, 2008
4 Ben-Omran T., "Phenotypic heterogeneity in Wood-house-Sakati syndrome: two new families with a mutation in the C2orf37 gene" 155A : 2647-2653, 2011
5 Hogarth P, "Neurodegeneration with brain iron accumula-tion : diagnosis and management" 8 : 1-13, 2015
6 Alazami AM., "Mutations in C2orf37, encoding a nucle-olar protein, cause hypogonadism, alopecia, diabetes mel-litus, mental retardation, and extrapyramidal syndrome" 83 : 684-691, 2008
7 Nanda A., "Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome : report of a family with mutation in the C2orf37 gene" 31 : 83-87, 2014
8 Woodhouse NJ., "A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities" 20 : 216-219, 1983
9 Habib R., "A novel splice site mutation in gene C2orf37 underlying Wood-house-Sakati syndrome(WSS)in a consanguineous family of Pakistani origin" 490 : 26-31, 2011
10 Steindl K., "A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome" 78 : 594-597, 2010