Gene responsible for mitochondrial myopathy and sideroblastic anemia (MSA) maps to chromosome 12q24.33

American Journal of Medical Genetics

Volumn 127 A, Issue 1, 2004, Pages 44-49

  Casas, Kari ^a   Bykhovskaya, Yelena ^a   Mengesha, Emebet ^a   Wang, Dai ^a   Yang, Huiying ^a   Taylor, Kent ^a   Inbal, Aida ^b   Fischel Ghodsian, Nathan ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

Autosomal recessive; Homozygosity; Mitochondrial myopathy; Sideroblastic anemia

Indexed keywords

ADOLESCENT; ADULT; ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BLOOD TRANSFUSION; CHROMOSOME 12Q; CLINICAL ARTICLE; DNA DETERMINATION; FAMILY; FEMALE; GENE EXPRESSION; GENE FUNCTION; GENE IDENTIFICATION; GENE MAPPING; GENETIC LINKAGE; GENETIC VARIABILITY; GENOME ANALYSIS; HOMOZYGOSITY; HUMAN; IRAN; IRON METABOLISM; JEW; LINKAGE ANALYSIS; MALE; MITOCHONDRIAL MYOPATHY; MUSCLE WEAKNESS; NUCLEOTIDE SEQUENCE; OXIDATIVE PHOSPHORYLATION; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; SCORING SYSTEM; SIDEROBLASTIC ANEMIA; TISSUE SPECIFICITY; UNITED STATES;

GENETTA; IRANIA;

EID: 3142696191     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20652     Document Type: Article

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