A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice

Genes and Development

Volumn 15, Issue 6, 2001, Pages 652-657

  Fleming, Mark D ^a,b   Campagna, Dean R ^a   Haslett, Judith N ^a   Trenor III, Cameron C ^a   Andrews, Nancy C ^a,b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Anemia; Flexed tail; Iron; Mitochondria; Mouse; Sideroblast

Indexed keywords

MEMBRANE PROTEIN;

ARTICLE; BIOSYNTHESIS; CHROMOSOME 13; CONTROLLED STUDY; EUKARYOTE; FRAMESHIFT MUTATION; GENE MUTATION; IMMUNOBLOTTING; IRON METABOLISM; MOUSE; MULTIGENE FAMILY; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANIMALS; BLOTTING, NORTHERN; BLOTTING, WESTERN; BONE AND BONES; CATION TRANSPORT PROTEINS; CELL LINE; CELL MEMBRANE; CLONING, MOLECULAR; DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; FRAMESHIFT MUTATION; HUMANS; MEMBRANE PROTEINS; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MITOCHONDRIA; MODELS, GENETIC; MOLECULAR SEQUENCE DATA; OPEN READING FRAMES; PHENOTYPE; PHYSICAL CHROMOSOME MAPPING; SEQUENCE HOMOLOGY, AMINO ACID; TISSUE DISTRIBUTION;

ANIMALIA; EUKARYOTA; MAMMALIA;

EID: 0035868772     PISSN: 08909369     EISSN: None     Source Type: Journal    
DOI: 10.1101/gad.873001     Document Type: Article

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