A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis

Blood

Volumn 99, Issue 8, 2002, Pages 3066-3069

  Arcasoy, Murat O ^a,b   Karayal, Aysen F ^a,b   Segal, Harvey M ^a,b   Sinning, Joseph G ^a,b   Forget, Bernard G ^a,b  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROPOIETIN; ERYTHROPOIETIN RECEPTOR; METHYLCELLULOSE;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CARBOXY TERMINAL SEQUENCE; CLINICAL ARTICLE; CONTROLLED STUDY; ERYTHROCYTOSIS; ERYTHROID PRECURSOR CELL; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HETEROZYGOSITY; HUMAN; MALE; MYELOPROLIFERATIVE DISORDER; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

EID: 0037089336     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V99.8.3066     Document Type: Article

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