Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene

Autor:	Alexandra Katsarou, Emmanuel Kanavakis, Christine Vrettou, Patrick Willems, Eleni Leze, Sofia Kitsiou-Tzeli, Maria Kosmadaki
Rok vydání:	2011
Předmět:	Basal (phylogenetics) Pathology medicine.medical_specialty Ptch gene business.industry Carcinoma medicine Dermatology General Medicine medicine.disease business Novel mutation
Zdroj:	The Journal of Dermatology. 38:1205-1208
ISSN:	0385-2407
DOI:	10.1111/j.1346-8138.2011.01265.x
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::49964505155863bbe6e4c983075c71be https://doi.org/10.1111/j.1346-8138.2011.01265.x Zobrazit plný text záznamu Plný text