De novomutation in theKCNQ1gene causal to Jervell and Lange-Nielsen syndrome-Reference-Cited by-同舟云学术

De novomutation in theKCNQ1gene causal to Jervell and Lange-Nielsen syndrome

Author:

Al-Aama J.Y.¹²,Al-Ghamdi S.³,Bdier A.Y.²,Wilde A.A.M.²⁴,Bhuiyan Zahurul A.⁵

Affiliation:

1. Department of Genetic Medicine; King Abdulaziz University Hospital; Jeddah Saudi Arabia

2. Princess Al Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders; King Abdulaziz University; Jeddah Saudi Arabia

3. Department of Pediatric Cardiology; Prince Sultan Cardiac Center; Riyadh Saudi Arabia

4. Department of Cardiology, Academic Medical Center; University of Amsterdam; Amsterdam the Netherlands

5. Laboratoire de Génétique Moléculaire, Service de Génétique Médicale; CHUV; Lausanne Switzerland

Funder

King Abdulaziz City for Science and Technology (KACST)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference26 articles.

4. The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome;Denjoy;Arch Mal Coeur Vaiss,2007

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