Clinical features and WNT 10A mutations in seven unrelated cases of Schöpf–Schulz–Passarge syndrome-Reference-Cited by-同舟云学术

Clinical features and WNT 10A mutations in seven unrelated cases of Schöpf–Schulz–Passarge syndrome

Published:2014-10-15 Issue:5 Volume:171 Page:1211-1214
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Tziotzios C.¹,Petrof G.¹,Liu L.¹,Verma A.¹,Wedgeworth E.K.¹,Mellerio J.E.¹,McGrath J.A.¹

Affiliation:

1. St. John's Institute of Dermatology King's College London (Guy's Campus) London SE1 9RT U.K

Funder

Department of Health via the UK National Institute for Health Research NIHR Comprehensive Biomedical Research Centre award to Guy's & St Thomas’ NHS Foundation Trust

King's College London and King's College Hospital NHS Foundation Trust

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.13158

Reference15 articles.

1. Wnt Signaling: Multiple Pathways, Multiple Receptors, and Multiple Transcription Factors

2. Continuous tooth generation in mouse is induced by activated epithelial Wnt/beta-catenin signaling

3. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

4. Schöpf–Schulz–Passarge syndrome: further delineation of the phenotype and genetic considerations;Castori M;Acta Derm Venereol,2008

5. Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal Dysplasia

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