Ann Dermatol.
2019 Aug;31(Suppl 1):S10-S11. 10.5021/ad.2019.31.S.S10.
Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
- Affiliations
-
- 1Department of Dermatology, Duzce University, Duzce, Turkey. dermatologg@gmail.com
- 2Department of Dermatology, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.
- 3Department of Medical Genetics, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.
- 4Department of Medical Genetics, Bezmialem University School of Medicine, Istanbul, Turkey.
- 5Department of Pathology, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.
- KMID: 2456634
- DOI: http://doi.org/10.5021/ad.2019.31.S.S10
Abstract
- No abstract available.
MeSH Terms
- Full Text Links
-
- Actions
-
Cited
- CITED
-
- Close
- Share
-
- Similar articles
-
- The First Korean Case of Gorlin?Goltz Syndrome Caused by a PTCH2 Pathogenic Variant Identified via Whole Exome Sequencing
- Novel Patched 1 Mutations in Patients with Gorlin-Goltz Syndrome Strategic Treated by Smoothened Inhibitor
- Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome
- Radiological features of familial Gorlin-Goltz syndrome
- Imaging findings in a case of Gorlin-Goltz syndrome: a survey using advanced modalities
