A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome

Nature Genetics

Volumn 28, Issue 4, 2001, Pages 345-349

  Zhou, Bing ^a   Westaway, Shawn K ^b   Levinson, Barbara ^a   Johnson, Monique A ^b   Gitschier, Jane ^a   Hayflick, Susan J ^b  

^a HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PANTOTHENATE KINASE;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; CLINICAL FEATURE; GENE MUTATION; GENETIC LINKAGE; HALLERVORDEN SPATZ DISEASE; HUMAN; IRON METABOLISM; PATHOGENESIS; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BRAIN; CAENORHABDITIS ELEGANS; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, PAIR 5; CODON, INITIATOR; DNA MUTATIONAL ANALYSIS; DROSOPHILA MELANOGASTER; GENES, RECESSIVE; HALLERVORDEN-SPATZ SYNDROME; HUMANS; IRON; MICE; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; MUTATION; ORGAN SPECIFICITY; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); PHYSICAL CHROMOSOME MAPPING; SACCHAROMYCES CEREVISIAE; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; TERMINOLOGY;

EID: 0034935036     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng572     Document Type: Article

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