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Novel mutation in the PTCH 1 gene in a patient with Gorlin syndrome with prominent clinical features
Author(s) -
ValdivielsoRamos M.,
Solera J.,
Mauleon C.,
Hernanz J. M.,
Amiñoso C.,
Galiano S.,
la Cueva P.
Publication year - 2014
Publication title -
clinical and experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 78
eISSN - 1365-2230
pISSN - 0307-6938
DOI - 10.1111/ced.12291
Subject(s) - medicine , dermatology