Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability

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Bibliographic Details
Main Authors: Zombor Melinda
Kalmár Tibor
Maróti Zoltán
Zimmermann Aliz
Máté Adrienn
Bereczki Csaba
Sztriha László
Format: Article
Published: 2018
Series:JOURNAL OF HUMAN GENETICS 63 No. 11
doi:10.1038/s10038-018-0508-x

mtmt:30316417
Online Access:http://publicatio.bibl.u-szeged.hu/15082
Description
Physical Description:1189-1193
ISSN:1434-5161