Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families-Reference-Cited by-同舟云学术

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Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families

Published:2016-04-06 Issue:10 Volume:24 Page:1430-1435
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Issa Yasmin A,Kamal Lara,Rayyan Amal Abu,Dweik Dima,Pierce Sarah,Lee Ming K,King Mary-Claire,Walsh Tom,Kanaan Moien

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg201629.pdf

Reference31 articles.

1. Nieminen P : Genetic basis of tooth agenesis. J Exp Zool B Mol Dev Evol 2009; 312B: 320–342.

2. Massink MP, Créton MA, Spanevello F et al: Loss-of-function mutations in the WNT co-receptor LRP6 cause autosomal-dominant oligodontia. Am J Hum Genet 2015; 97: 621–626.

3. Arte S, Nieminen P, Apajalahti S, Haavikko K, Theslef I, Pirinen S : Characteristics of incisor-premolar hypodontia in families. J Dental Res 2001; 80: 1445–1450.

4. Visinoni AF, Lisboa-Costa T, Pagnan NA, Chautard-Freire-Maia EA : Ectodermal dysplasias: clinical and molecular review. Am J Med Genet Part A 2009; 149A: 1980–2002.

5. DeCoster PJ, Marks LA, Martens LC, Huysseune A : Dental agenesis: genetic and clinical perspectives. J Oral Pathol Med 2009; 38: 1–17.

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