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: identification of a U2HR mutation in the family from the original 1925 report.
Redler S et al.
Journal of the American Academy of Dermatology, 2011
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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