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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family

Year of publication

2016

Authors

Callea, M.; Nieminen, P.; Willoughby, C. E.; Clarich, G.; Yavuz, I.; Vinciguerra, A.; Di Stazio, M.; Giglio, S.; Sani, I.; Maglione, M.; Pensiero, S.; Tadini, G.; Bellacchio, E.

Organizations and authors

Publication type

Publication format

Article

Parent publication type

Journal

Article type

Original article

Audience

Scientific

Peer-reviewed

Peer-Reviewed

MINEDU's publication type classification code

A1 Journal article (refereed), original research

Publication channel information

Volume

30

Issue

2

Pages

341-343

​Publication forum

61880

​Publication forum level

1

Open access

Open access in the publisher’s service

No

Self-archived

No

Other information

Fields of science

General medicine, internal medicine and other clinical medicine

Publication country

United Kingdom

Internationality of the publisher

International

Language

English

International co-publication

Yes

Co-publication with a company

No

DOI

10.1111/jdv.12747

The publication is included in the Ministry of Education and Culture’s Publication data collection

Yes