Identification of aU2HRgene mutation in Turkish families with Marie Unna hereditary hypotrichosis
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.2009.03644.x/fullpdf
Reference9 articles.
1. Ãber Hypotrichosis congenita hereditaria;Unna;Dermatol Wochenschr,1925
2. Marie Unna hypotrichosis in an Asian family;Kim;J Dermatol,2001
3. Marie Unna hypotrichosis in a Chinese family;Wong;Pediatr Dermatol,2002
4. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family;Cichon;Br J Dermatol,2000
5. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing;van Steensel;Am J Hum Genet,1999
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1. Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report;European Journal of Dermatology;2018-05
2. Identification of mutations inU2HRin two Chinese families with Marie Unna hereditary hypotrichosis;Clinical and Experimental Dermatology;2015-08-12
3. Did human hairlessness allow natural photobiomodulation 2 million years ago and enable photobiomodulation therapy today? This can explain the rapid expansion of our genus’s brain;Medical Hypotheses;2015-05
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5. The regulatory potential of upstream open reading frames in eukaryotic gene expression;Wiley Interdisciplinary Reviews: RNA;2014-07-03
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