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mutations may cause a mutation-negative Rett syndrome phenotype.

作者信息

Kulikovskaja Leonora, Sarajlija Adrijan, Savic-Pavicevic Dusanka, Dobricic Valerija, Klein Christine, Westenberger Ana

机构信息

Institute of Neurogenetics (L.K., C.K., A.W.), University of Lübeck, Germany; Department of Metabolism and Clinical Genetics (A.S.), Mother and Child Health Care Institute of Serbia, Belgrade; Centre for Human Molecular Genetics (D.S.-P.), Faculty of Biology, University of Belgrade, Serbia; and Lübeck Interdisciplinary Platform for Genome Analytics (LIGA) (V.D.), University of Lübeck, Germany.

出版信息

Neurol Genet. 2018 Mar 27;4(2):e227. doi: 10.1212/NXG.0000000000000227. eCollection 2018 Apr.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e31e/5873728/4ffd77957bbe/NG2017007039FF1.jpg

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