Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5(Hum Genet, DOI:10.1007/s00439-014-1522-5);Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

Human Genetics

Volumn 134, Issue 3, 2015, Pages 305-314

  Magen, Daniella ^a,b   Ofir, Ayala ^b   Berger, Liron ^b   Goldsher, Dorit ^b,c   Eran, Ayelet ^b,c   Katib, Nassser ^d   Nijem, Yousif ^e   Vlodavsky, Euvgeni ^b,c   Zur, Shay ^b   Behar, Doron M ^b   Fellig, Yakov ^f   Mandel, Hanna ^b,g  

^a Pediatric Nephrology Unit   (Israel)

^b TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^c Clalit Health Services ^*  (Israel)

^d CLALIT HEALTH SERVICES   (Israel)

^e Nazareth Hospital   (Israel)

^f HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^g Metabolic Bone Diseases Unit   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN DEPENDENT KINASE 5; GALACTOSE; GLUCOSE; CDK5 PROTEIN, HUMAN;

ACTIN FILAMENT; AGYRIA; ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE LISSENCEPHALY; BRAIN TISSUE; CARBON SOURCE; CASE REPORT; CELL SHAPE; CELL STRUCTURE; CEREBELLUM HYPOPLASIA; CHROMOSOME; CONTROLLED STUDY; DAUGHTER CELL; EXOME; EXON; GENE EXPRESSION; GENE PRODUCT; GENETIC ASSOCIATION; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INFANT; ISRAELI; LOSS OF FUNCTION MUTATION; MUSLIM; NEWBORN; NONSENSE MEDIATED MRNA DECAY; NORTHERN BLOTTING; OPEN READING FRAME; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SEQUENCE; SEQUENCE ANALYSIS; SKIN FIBROBLAST; STOP CODON; YEAST CELL; ABNORMALITIES; CELL CULTURE; CEREBELLUM; CONSANGUINITY; DEVELOPMENTAL DISORDER; DNA MUTATIONAL ANALYSIS; ENZYMOLOGY; FEMALE; GENETIC ASSOCIATION STUDY; GENETIC COMPLEMENTATION; GENETICS; HOMOZYGOTE; MALE; MISSENSE MUTATION; NERVOUS SYSTEM MALFORMATION; NUCLEOTIDE SEQUENCE; PEDIGREE; RECESSIVE GENE;

BASE SEQUENCE; CELLS, CULTURED; CEREBELLUM; CONSANGUINITY; CYCLIN-DEPENDENT KINASE 5; DEVELOPMENTAL DISABILITIES; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, RECESSIVE; GENETIC ASSOCIATION STUDIES; GENETIC COMPLEMENTATION TEST; HOMOZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; LISSENCEPHALY; MALE; MUTATION, MISSENSE; NERVOUS SYSTEM MALFORMATIONS; PEDIGREE;

EID: 84938248071     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-015-1530-0     Document Type: Erratum

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