A novel <i>de novo</i> heterozygous variant of the KCNQ2 gene: Contribution to early‑onset epileptic encephalopathy in a female infant-Reference-Cited by-同舟云学术

A novel de novo heterozygous variant of the KCNQ2 gene: Contribution to early‑onset epileptic encephalopathy in a female infant

Published:2022-07-19 Issue:3 Volume:26 Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Rep

Author:

Liu Hai-Feng¹,Yuan Ting-Yun¹,Yang Jia-Wu¹,Li Feng¹,Wang Fan¹,Fu Hong-Min¹

Affiliation:

1. Department of Pulmonary and Critical Care Medicine, Kunming Children's Hospital and Yunnan Key Laboratory of Children's Major Disease Research, Kunming, Yunnan 650034, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Reference53 articles.

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5. CDKL5 deficiency disorder-A complex epileptic encephalopathy;Jakimiec;Brain Sci,2020

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