Caricamento...
A novel PTCH1 mutation in a patient with Gorlin syndrome
Gorlin syndrome is an autosomal dominant disorder characterized by a wide range of developmental abnormalities and a predisposition to various tumors, and it is linked to the alteration of several causative genes, including PTCH1. We performed targeted resequencing using a next-generation sequencer...
Salvato in:
| Pubblicato in: | Hum Genome Var |
|---|---|
| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group
2014
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4785514/ https://ncbi.nlm.nih.gov/pubmed/27081512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2014.22 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|