Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene
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Published in | Molecular syndromology Vol. 13; no. 1; pp. 56 - 63 |
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Main Authors | , |
Format | Report |
Language | English |
Published |
01.02.2022
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Online Access | Get full text |
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Bibliography: | ObjectType-Case Study-2 content type line 59 SourceType-Reports-1 ObjectType-Report-1 |
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ISSN: | 1661-8769 |
DOI: | 10.1159/000516201 |