Novel approaches to studying the genetic basis of cerebellar development

Cerebellum

Volumn 9, Issue 3, 2010, Pages 272-283

  Sajan, Samin A ^a   Waimey, Kathryn E ^a   Millen, Kathleen J ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

Ataxia; Cerebellum; Congenital human cerebellar malformations; Genetics; Genomics; Neurological and targeted mouse mutants

Indexed keywords

BRAIN DEVELOPMENT; BRAIN MALFORMATION; CEREBELLUM DEVELOPMENT; CEREBELLUM DISEASE; CEREBELLUM MALFORMATION; CEREBELLUM VERMIS HYPOPLASIA; DEVELOPMENTAL GENE; GENE DOSAGE; GENE IDENTIFICATION; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; JOUBERT SYNDROME; MUTANT; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; PONTOCEREBELLAR HYPOPLASIA; PRIORITY JOURNAL; PROTEOMICS; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

ANIMALS; CEREBELLUM; GENETIC TECHNIQUES; HUMANS; MICE; MICE, MUTANT STRAINS;

EID: 78049260010     PISSN: 14734222     EISSN: 14734230     Source Type: Journal    
DOI: 10.1007/s12311-010-0169-6     Document Type: Review

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