Tricho-odonto-onycho-dermal dysplasia andWNT10Amutations-Reference-Cited by-同舟云学术

Tricho-odonto-onycho-dermal dysplasia andWNT10Amutations

Published:2014-01-23 Issue:4 Volume:164 Page:1041-1048
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kantaputra P.¹²³⁴,Kaewgahya M.²⁴,Jotikasthira D.⁵,Kantaputra W.²³

Affiliation:

1. Division of Pediatric Dentistry; Department of Orthodontics and Pediatric Dentistry; Faculty of Dentistry; Chiang Mai University; Chiang Mai Thailand

2. Craniofacial Genetics Laboratory; Faculty of Dentistry; Chiang Mai University; Chiang Mai Thailand

3. Dentaland Clinic; Chiang Mai Thailand

4. Center of Excellence in Medical Genetics Research; Chiang Mai University; Chiang Mai Thailand

5. Division of Orthodontics, Department of Orthodontics and Pediatric Dentistry; Faculty of Dentistry; Chiang Mai University; Chiang Mai Thailand

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia;Adaimy;Am J Hum Genet,2007

2. Variant of odontoonychodermal dysplasia;Arnold;Am J Med Genet Part A,1995

3. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes;Bohring;Am J Hum Genet,2009

4. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia;Calvas;Am J Med Genet Part A,2013

5. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases;Cluzeau;Hum Mutat,2011

Cited by 29 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. Inherited Disorders of Cornification;Rook's Textbook of Dermatology;2024-03-19

2. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia;BMC Oral Health;2024-01-27

3. Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review;Dentistry Journal;2023-12-04

4. Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss;British Journal of Dermatology;2023-09-06

5. PAX9 mutations and genetic synergism in familial tooth agenesis;Annals of the New York Academy of Sciences;2023-04-02