Spectrum ofPTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: Identification of thirteen novel alleles-Reference-Cited by-同舟云学术

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Spectrum ofPTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: Identification of thirteen novel alleles

Published:2004 Issue:5 Volume:24 Page:441-441
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Savino Maria,d'Apolito Maria,Formica Vincenza,Baorda Filomena,Mari Francesca,Renieri Alessandra,Carabba Enrico,Tarantino Enrico,Andreucci Elena,Belli Serena,Muzio Lorenzo Lo,Dallapiccola Bruno,Zelante Leopoldo,Savoia Anna

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Gorlin Syndrome: Recent Advances in Genetic Testing and Molecular and Cellular Biological Research;International Journal of Molecular Sciences;2020-10-13

2. Novel PTCH1 mutation in Gorlin–Goltz syndrome potentially altered interactions with lipid bilayer;Oral Diseases;2020-08-31

3. The Role of Dermal Fibroblasts in Nevoid Basal Cell Carcinoma Syndrome Patients: An Overview;International Journal of Molecular Sciences;2020-01-22

4. A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome;Medical Molecular Morphology;2019-04-17

5. Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome;British Journal of Dermatology;2017-12-22

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