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Neurogenetics|July 26, 2018
Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelinationTamar Harel, Debra Q Y Quek, Bernice H Wong, et al.Neurology|March 31, 2015
Copy number variations in cryptogenic cerebral palsyReeval Segel, Hilla Ben-Pazi, Sharon Zeligson, et al.Journal of Medical Genetics|July 29, 2021
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsyMichal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.Pageof 2