The wooly mutation (wly) on mouse chromosome 11 is associated with a genetic defect in Fam83g

BMC Research Notes

Volumn 6, Issue 1, 2013, Pages

  Radden, Legairre A ^a   Child, Kevin M ^a   Adkins, Elisabeth B ^a   Spacek, Damek V ^a   Feliciano, Aaron M ^a   King, Thomas R ^a  

^a CENTRAL CONNECTICUT STATE UNIVERSITY   (United States)

Author keywords

Fam83g; Hair variant; Mouse model; Positional candidate approach; Slc5a10

Indexed keywords

ANIMALIA; MAMMALIA; MUS;

FAM83G PROTEIN, MOUSE; PRIMER DNA; PROTEIN;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CHROMOSOME MAP; CROSS BREEDING; GENETICS; MEIOSIS; MOLECULAR GENETICS; MOLECULAR PROBE; MOUSE; MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; CROSSES, GENETIC; DNA PRIMERS; MEIOSIS; MICE; MOLECULAR PROBES; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 84877132765     PISSN: None     EISSN: 17560500     Source Type: Journal    
DOI: 10.1186/1756-0500-6-189     Document Type: Article

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