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

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
Human Genetics · Vol. 134, Issue 3 · pp. 305-314 · 2015

Abstract

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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2015-03-01
Publication Year2015
Volume134
Issue3
Pages305-314
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-014-1522-5

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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