Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene

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Bibliographic Details
Published inMolecular syndromology Vol. 13; no. 1; pp. 56 - 63
Main Authors Türkyılmaz, Ayberk, Sager, Safiye Gunes
Format Report
LanguageEnglish
Published 01.02.2022
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Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:1661-8769
DOI:10.1159/000516201