A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia

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Bibliographic Details
Main Authors: Kalmár Tibor
Szakszon Katalin
Maróti Zoltán
Zimmermann Aliz
Máté Adrienn
Zombor Melinda
Bereczki Csaba
Sztriha László
Format: Article
Published: 2021
Series:JOURNAL OF PEDIATRIC GENETICS 10 No. 2
doi:10.1055/s-0040-1712916

mtmt:31599322
Online Access:http://publicatio.bibl.u-szeged.hu/20149
Description
Physical Description:159-163
ISSN:2146-4596