Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia-Reference-Cited by-同舟云学术

Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia

Author:

Intarak N.¹,Theerapanon T.²,Srijunbarl A.³,Suphapeetiporn K.⁴⁵,Porntaveetus T.¹^ORCID,Shotelersuk V.⁴⁵

Affiliation:

1. Craniofacial Genetics and Stem Cells Research Group; Department of Physiology; Chulalongkorn University; Bangkok 10330 Thailand

2. Excellence Center in Regenerative Dentistry; Chulalongkorn University; Bangkok 10330 Thailand

3. Dental Material Science Research Center; Faculty of Dentistry; Chulalongkorn University; Bangkok 10330 Thailand

4. Center of Excellence for Medical Genetics; Department of Pediatrics; Faculty of Medicine; Chulalongkorn University; Bangkok 10330 Thailand

5. Excellence Center for Medical Genetics; King Chulalongkorn Memorial Hospital; the Thai Red Cross Society; Bangkok 10330 Thailand

Funder

Thailand Research Fund

Office of the Higher Education Commission

Ratchadapisek Sompot Fund for Postdoctoral Fellowship, Chulalongkorn University.

Faculty of Dentistry, Chulalongkorn University

Chulalongkorn Academic Advancement Into Its 2nd Century Project.

Publisher

Wiley

Subject

Dermatology

Link

Reference7 articles.

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