Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome

Detalles Bibliográficos
Autores principales: Ozlu, Emin, Karadag, Ayse Serap, Akalın, Ibrahim, Yesil, Gozde, Yılmaz, Sarenur, Zindancı, Ilkin, Uzuncakmak, Tugba Kevser, Ozkanlı, Seyma, Akdeniz, Necmettin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997056/
https://www.ncbi.nlm.nih.gov/pubmed/33911679
http://dx.doi.org/10.5021/ad.2019.31.S.S10
_version_ 1783670240906838016
author Ozlu, Emin
Karadag, Ayse Serap
Akalın, Ibrahim
Yesil, Gozde
Yılmaz, Sarenur
Zindancı, Ilkin
Uzuncakmak, Tugba Kevser
Ozkanlı, Seyma
Akdeniz, Necmettin
author_facet Ozlu, Emin
Karadag, Ayse Serap
Akalın, Ibrahim
Yesil, Gozde
Yılmaz, Sarenur
Zindancı, Ilkin
Uzuncakmak, Tugba Kevser
Ozkanlı, Seyma
Akdeniz, Necmettin
author_sort Ozlu, Emin
collection PubMed
description
format Online
Article
Text
id pubmed-7997056
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher The Korean Dermatological Association; The Korean Society for Investigative Dermatology
record_format MEDLINE/PubMed
spelling pubmed-79970562021-04-27 Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome Ozlu, Emin Karadag, Ayse Serap Akalın, Ibrahim Yesil, Gozde Yılmaz, Sarenur Zindancı, Ilkin Uzuncakmak, Tugba Kevser Ozkanlı, Seyma Akdeniz, Necmettin Ann Dermatol Brief Report The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019-08 2019-07-01 /pmc/articles/PMC7997056/ /pubmed/33911679 http://dx.doi.org/10.5021/ad.2019.31.S.S10 Text en Copyright © 2019 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Ozlu, Emin
Karadag, Ayse Serap
Akalın, Ibrahim
Yesil, Gozde
Yılmaz, Sarenur
Zindancı, Ilkin
Uzuncakmak, Tugba Kevser
Ozkanlı, Seyma
Akdeniz, Necmettin
Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
title Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
title_full Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
title_fullStr Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
title_full_unstemmed Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
title_short Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
title_sort novel ptch1 gene mutation in a patient with gorlin–goltz syndrome
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997056/
https://www.ncbi.nlm.nih.gov/pubmed/33911679
http://dx.doi.org/10.5021/ad.2019.31.S.S10
work_keys_str_mv AT ozluemin novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT karadagayseserap novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT akalınibrahim novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT yesilgozde novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT yılmazsarenur novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT zindancıilkin novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT uzuncakmaktugbakevser novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT ozkanlıseyma novelptch1genemutationinapatientwithgorlingoltzsyndrome
AT akdeniznecmettin novelptch1genemutationinapatientwithgorlingoltzsyndrome

Ejemplares similares