Wikidata

(Q58859826)

English

De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic Dermatitis

scientific article published on 15 November 2007

In more languages

Statements

title
De novo occurrence of the filaggrin mutation p.R501X with prevalent mutation c.3321delA in a Japanese family with ichthyosis vulgaris complicated by atopic dermatitis (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18007582
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18007582%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019

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