New homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree with Netherton syndrome.

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Bibliographic Details
Title: New homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree with Netherton syndrome.
Authors: Fong, K.1, Akdeniz, S.2, Isi, H.2, Taskesen, M.2, McGrath, J. A.1 john.mcgrath@kcl.ac.uk, Lai-Cheong, J. E.1
Source: Clinical & Experimental Dermatology. Jun2011, Vol. 36 Issue 4, p412-415. 4p. 1 Color Photograph, 1 Diagram.
Database: Academic Search Ultimate
Description
ISSN:03076938
DOI:10.1111/j.1365-2230.2010.03976.x