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A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia
Kalmár, Tibor, Szakszon, Katalin, Maróti, Zoltán, Zimmermann, AlÃz, Máté, Adrienn, Zombor, Melinda, Bereczki, Csaba, Sztriha, LászlóJournal:
Journal of Pediatric Genetics
DOI:
10.1055/s-0040-1712916
Date:
May, 2020
File:
PDF, 1.35 MB
2020