Molecular definition of an allelic series of mutations disrupting the mouse Lmx1a (dreher) gene

Mammalian Genome

Volumn 17, Issue 10, 2006, Pages 1025-1032

  Chizhikov, Victor ^a   Steshina, Ekaterina ^b   Roberts, Richard ^a   Ilkin, Yesim ^a   Washburn, Linda ^c   Millen, Kathleen J ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^c JACKSON LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; LIM PROTEIN; PROTEIN LMX1A; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ATAXIA; BEHAVIOR; BRAIN MALFORMATION; CEREBELLUM DISEASE; CONTROLLED STUDY; DANDY WALKER SYNDROME; FRAMESHIFT MUTATION; GENE DELETION; GENE DISRUPTION; GENE MUTATION; HOMEOBOX; HYPERACTIVITY; LMX1A GENE; MISSENSE MUTATION; MOLECULAR CLONING; MOUSE; NONHUMAN; NULL ALLELE; PHENOTYPE; SKELETON MALFORMATION; SKIN PIGMENTATION; VESTIBULAR DISORDER;

ALLELES; AMINO ACID SEQUENCE; ANIMALS; CEREBELLUM; DANDY-WALKER SYNDROME; DISEASE MODELS, ANIMAL; DNA MUTATIONAL ANALYSIS; HOMEODOMAIN PROTEINS; MICE; MICE, INBRED C57BL; MOLECULAR SEQUENCE DATA; MUTATION; SEQUENCE HOMOLOGY, AMINO ACID;

ATAXIA;

EID: 33749581676     PISSN: 09388990     EISSN: 14321777     Source Type: Journal    
DOI: 10.1007/s00335-006-0033-7     Document Type: Article

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