Work

Whole exome sequencing identifies a mutation for a novel form of hereditary benign intraepithelial dyskeratosis

Year: 2012

Type: conference-abstract

Source: Acta Ophthalmologica

DOI: 10.1111/j.1755-3768.2012.t060.x

Authors: V SOLER, KN TRAN‐VIET, E ST.GERMAIN, P FOURNIE, T KLEMM, F HAWTHORNE, NA AFSHARI, P CALVAS, F MALECAZE, T YOUNG

Institutions: Université Toulouse III - Paul Sabatier, Duke University, Hôpital Paule de Viguier, Hôpital Purpan, National University of Singapore, Duke-NUS Medical School, Duke University Hospital

Language: English

Topic: Genetic and rare skin diseases.

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1592538631

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