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Title: Hereditary Alopecia in Pakistani families
Authors: Ghazanfar Ali
Journal: Journal of Pakistan Medical Association
Publisher: Pakistan Medical Association.
Country: Pakistan
Year: 2010
Volume: 60
Issue: 10
Language: English
References
1.John P, Ali G, Chishti MS, Naqvi SM, Leal SM, Ahmad W. Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3. Hum Genet 2006; 118: 665-7.
2.Kazantseva A, Goltsov A, Zinchenko R, Grigorenko AP, Abrukova AV, Moliaka YK, et al. Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH. Science 2006; 314: 982-5.
3.Ali G, Chishti MS, Raza SI, John P, Ahmad W. A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis. Human Genetics 2007; 121: 319-25.
4.Jelani M, Wasif N, Ali G, Chishti MS, Ahmad W. A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2). Clin Genet 2008; 74: 184-8.
5.Azeem Z, Jelani M, Naz G, Tariq M, Wasif N, Kamran-Ul-Hassan Naqvi S, et al. Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). Hum Genet 2008; 123: 515-9.
6.Wali A, Ansar M, Khan MN, Ahmad W. Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene. Clin Exp Dermatol 2006; 31: 695-8.
7.Kljuic A, Gilead L, Martinez-Mir A, Frank J, Christiano AM, Zlotogorski A. A nonsense mutation in the desmoglein 1 gene underlies striate keratoderma. Exp Dermatol 2003; 12: 523-7.
8.John P, Tariq M, Arshad Rafiq M, Amin-Ud-Din M, Muhammad D, Waheed I, et al. Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins. Arch Dermatol Res 2006; 298: 135-7.
9.Wajid M, Bazzi H, Rockey J, Lubetkin J, Zlotogorski A, Christiano AM. Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family. J Invest Dermatol 2007; 127: 1779-82.
10.Wali A, John P, Gul A, Lee K, Chishti MS, Ali G, et al. A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31. Clin Genet 2006; 70: 233-9.
11.Wali A, Chishti MS, Ayub M, Yasinzai M, Kafaitullah K, Ali G, et al. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32. Clin Genet 2007; 72: 23-9.
12.Wali A, Ali G, John P, Lee K, Chishti MS, Leal SM, et al. Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2. Ann Hum Genet 2007; 71: 570-7.
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