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Erratum: Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

scholarly article published in Nature Genetics

Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance

artículo científico publicado en 2012

Genetic variants in CTLA4 are strongly associated with alopecia areata

article

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

artículo científico publicado en 2005

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

artículo científico publicado en 2011

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26

artículo científico publicado en 2008

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

artículo científico publicado en 2003

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

article

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

artículo científico publicado en 2009

Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia

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Susceptibility variants for male-pattern baldness on chromosome 20p11.

artículo científico publicado en 2008

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