Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features-Reference-Cited by-同舟云学术

Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features

Published:2018-07-25 Issue:10 Volume:63 Page:1077-1082
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Jaouadi Hager^ORCID,Kraoua Lilia,Chaker Lilia,Atkinson Alexandre^ORCID,Delague Valérie,Levy Nicolas,Benkhalifa Rym,Mrad Ridha,Abdelhak Sonia,Zaffran Stéphane^ORCID

Funder

Fondation Aix-Marseille Universite

Université de Tunis

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/s10038-018-0492-1.pdf

Reference15 articles.

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3. Wilkinson JD, Sleeper LA, Alvarez JA, Bublik N, Lipshultz SE. The Pediatric Cardiomyopathy Registry: 1995–2007. Prog Pediatr Cardiol. 2008;25:31–6.

4. Kindel SJ, Miller EM, Gupta R, Cripe LH, Hinton RB, Spicer RL, et al. Pediatric cardiomyopathy: importance of genetic and metabolic evaluation. J Card Fail. 2012;18:396–403.

5. Wilkinson JD, Westphal JA, Bansal N, Czachor JD, Razoky H, Lipshultz SE. Lessons learned from the Pediatric Cardiomyopathy Registry (PCMR) Study Group. Cardiol Young. 2015;25(Suppl 2):140–53.

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