Parental germline mosaicism in SCN3A-related severe developmental disorder.

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Bibliographic Details
Title: Parental germline mosaicism in SCN3A-related severe developmental disorder.
Authors: Inuzuka LM; Epilepsy Clinic, Hospital Sírio-Libanês, São Paulo, Brazil; Department of Neurology, University of São Paulo School of Medicine, Brazil. Electronic address: lminuzuka@gmail.com., Macedo-Souza LI; Department of Neurology, University of São Paulo School of Medicine, Brazil., Guerra-Peixe M; Department of Neurology, University of São Paulo School of Medicine, Brazil., Cobas Pedreira C; Epilepsy Clinic, Hospital Sírio-Libanês, São Paulo, Brazil; Department of Neurology, University of São Paulo School of Medicine, Brazil., Della-Ripa B; Department of Neurology, University of São Paulo School of Medicine, Brazil., Souza Delgado D; Radiology Department, Hospital Sírio-Libanês, São Paulo, Brazil., Monteiro F; Mendelics Genomic Analysis, São Paulo, Brazil., Kitajima JP; Mendelics Genomic Analysis, São Paulo, Brazil., Garzon E; Epilepsy Clinic, Hospital Sírio-Libanês, São Paulo, Brazil; Department of Neurology, University of São Paulo School of Medicine, Brazil., Kok F; Department of Neurology, University of São Paulo School of Medicine, Brazil; Mendelics Genomic Analysis, São Paulo, Brazil.
Source: Brain & development [Brain Dev] 2021 May; Vol. 43 (5), pp. 669-670. Date of Electronic Publication: 2021 Jan 22.
Publication Type: Letter
Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 7909235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-7131 (Electronic) Linking ISSN: 03877604 NLM ISO Abbreviation: Brain Dev Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1872-7131
DOI:10.1016/j.braindev.2020.12.013