A Trp33arg mutation at exon 1 of the MYH9 gene in a Korean patient with May-Hegglin Anomaly

Yonsei Medical Journal

Volumn 53, Issue 3, 2012, Pages 662-666

  Jang, Moon Ju ^a   Park, Hyun Jeong ^a   Chong, So Young ^a   Huh, Ji Young ^b   Kim, In Ho ^c   Jang, Ja Hyun ^a   Kim, Hee Jin ^a,d   Oh, Doyeun ^a  

^a Department of 1Internal Medicine ^*  (South Korea)

^b CHA University   (South Korea)

^c Seoul National University College of Medicine   (South Korea)

^d Sungkyunkwan University School of Medicine   (South Korea)

Author keywords

Korean; May hegglin anomaly; MYH9; Thrombocytopenia

Indexed keywords

ARGININE; MYOSIN; MYOSIN HEAVY CHAIN 9; TRYPTOPHAN; UNCLASSIFIED DRUG;

ADULT; ARTICLE; BASOPHIL; CASE REPORT; CODON; EXON; FAMILY HISTORY; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; HUMAN; KOREA; MALE; MAY HEGGLIN ANOMALY; THROMBOCYTE COUNT; THROMBOCYTOPENIA;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; EXONS; HUMANS; MALE; MOLECULAR MOTOR PROTEINS; MUTATION; MYOSIN HEAVY CHAINS; THROMBOCYTOPENIA; YOUNG ADULT;

EID: 84859766750     PISSN: 05135796     EISSN: None     Source Type: Journal    
DOI: 10.3349/ymj.2012.53.3.662     Document Type: Article

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