A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia
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Main Authors: | |
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Format: | Article |
Published: |
2021
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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 |
Physical Description: | 159-163 |
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ISSN: | 2146-4596 |