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Year | Number of Results |
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1998 | 1 |
2009 | 2 |
2024 | 0 |
PubMed for id: 193290130
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Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
Clin Exp Dermatol. 2009 Dec;34(8):e953-6. doi: 10.1111/j.1365-2230.2009.03644.x.
Clin Exp Dermatol. 2009.
PMID: 20055871
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
Wen Y, Liu Y, Xu Y, Zhao Y, Hua R, Wang K, Sun M, Li Y, Yang S, Zhang XJ, Kruse R, Cichon S, Betz RC, Nöthen MM, van Steensel MA, van Geel M, Steijlen PM, Hohl D, Huber M, Dunnill GS, Kennedy C, Messenger A, Munro CS, Terrinoni A, Hovnanian A, Bodemer C, de Prost Y, Paller AS, Irvine AD, Sinclair R, Green J, Shang D, Liu Q, Luo Y, Jiang L, Chen HD, Lo WH, McLean WH, He CD, Zhang X.
Wen Y, et al.
Nat Genet. 2009 Feb;41(2):228-33. doi: 10.1038/ng.276. Epub 2009 Jan 4.
Nat Genet. 2009.
PMID: 19122663
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Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.
Cichon S, Anker M, Vogt IR, Rohleder H, Pützstück M, Hillmer A, Farooq SA, Al-Dhafri KS, Ahmad M, Haque S, Rietschel M, Propping P, Kruse R, Nöthen MM.
Cichon S, et al.
Hum Mol Genet. 1998 Oct;7(11):1671-9. doi: 10.1093/hmg/7.11.1671.
Hum Mol Genet. 1998.
PMID: 9736769
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