Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability
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Main Authors: | |
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Format: | Article |
Published: |
2018
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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 |
Physical Description: | 1189-1193 |
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ISSN: | 1434-5161 |