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List of works by Yaran Wen

Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia

article

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

scientific article published on 4 January 2009

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

South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin

scientific article published on January 2014

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