Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene

Human Molecular Genetics

Volumn 12, Issue 10, 2003, Pages 1163-1170

  Davy, Brian E ^a   Robinson, Michael L ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; CALDESMON; COMPLEMENTARY DNA; CYTOSINE; GENOMIC DNA; GUANINE; MESSENGER RNA; MUTANT PROTEIN; PROTEIN HYDIN; UNCLASSIFIED DRUG;

ALLELE; AMINO ACID SEQUENCE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BASE PAIRING; BRAIN FOURTH VENTRICLE; BRAIN THIRD VENTRICLE; BRONCHUS; CHROMOSOME 8; CILIATED EPITHELIUM; CODON; CONGENITAL HYDROCEPHALUS; CONTROLLED STUDY; EPENDYMA CELL; EXON; FRAMESHIFT MUTATION; GENE DELETION; GENE EXPRESSION; GENE IDENTIFICATION; GENE INSERTION; GENE LOCUS; GENE LOSS; GENE REARRANGEMENT; GENETIC CODE; GENETIC SELECTION; GENETIC TRANSCRIPTION; HOMOZYGOTE; MOUSE; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; OVIDUCT; PRIORITY JOURNAL; PROTEIN INTERACTION; SEQUENCE HOMOLOGY; SPERMATOCYTE; TESTIS DEVELOPMENT; TRANSCRIPTION TERMINATION; TRANSGENE; WILD TYPE;

ANIMALS; BRAIN; FRAMESHIFT MUTATION; HYDROCEPHALUS; MALE; MICE; MICROFILAMENT PROTEINS; TESTIS;

ANIMALIA; BRONCHUS; INSERTION SEQUENCES;

EID: 0038778365     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddg122     Document Type: Article

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