ATP8A2 and AKAP10 Gene Mutations in a Patient with Prader-Willi Syndrome: A Case Report and Literature Review

Wu, KM; Tang, YF; Zhou, Q; Zou, CC

Zou, CC (corresponding author), Zhejiang Univ, Sch Med, Childrens Hosp, Dept Endocrinol, Hangzhou, Peoples R China.

IRANIAN JOURNAL OF PEDIATRICS, 2020; 30 (4):

Abstract

Introduction: Prader-Willi syndrome (PWS) is an epigenetic disease. Cerebellar ataxia, mental retardation, and disequilibrium syndrome type 4 (CAMRQ4)......

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