Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

Authors:	Daniella Magen Ayala Ofir Liron Berger Dorit Goldsher Ayelet Eran Nassser Katib Yousif Nijem Euvgeni Vlodavsky Shay Zur Doron M. Behar Yakov Fellig Hanna Mandel

Affiliation:	1. Pediatric Nephrology Institute, Rambam Health Care Campus, Haifa, Israel 2. Laboratory of Molecular Medicine, the Rappaport Faculty of Medicine and Research Institute, Technion-Israel Institute of Technology, Haifa, Israel 3. Department of Diagnostic Imaging, Rambam Health Care Campus, Haifa, Israel 4. The Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel 5. Department of Family Medicine, Clalit Health Services, Ozer, Lower Galilee, Israel 6. Pediatric and Neonatal Unit, Nazareth Hospital EMMS, Nazareth, Israel 7. Department of Pathology, Rambam Health Care Campus, Haifa, Israel 8. Department of Pathology, Hadassah Hebrew University Medical Center, Jerusalem, Israel 9. Metabolic Unit, Rambam Health Care Campus, Haifa, Israel

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