Associated Papers
Genetics of human isolated hereditary hair loss disorders.
Basit S et al.
Clinical Genetics, 2015
25350920 (PubMed )
Supplement: supplement_1.pdf
Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.
Yun SK et al.
International Journal of Dermatology, 2014
Marie Unna hereditary hypotrichosis: a recurrent c.74C>T mutation in the U2HR gene and literature review.
Yang J et al.
International Journal of Dermatology, 2014
Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutation.
Mansur AT et al.
American Journal of Medical Genetics. Part A, 2010
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
Düzenli S et al.
Clinical and Experimental Dermatology, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
Wen Y et al.
Nature Genetics, 2009
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