Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)

Blood

Volumn 97, Issue 4, 2001, Pages 1147-1149

  Kunishima, S ^a   Kojima, T ^a   Matsushita, T ^a   Tanaka, T ^a   Tsurusawa, M ^a   Furukawa, Y ^a   Nakamura, Y ^a   Okamura, T ^a   Amemiya, N ^a   Nakayama, T ^a   Kamiya, T ^a   Saito, H ^a  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN HEAVY CHAIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL INCLUSION; GENE DELETION; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE; MAY HEGGLIN ANOMALY; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEBASTIAN SYNDROME; THROMBOCYTOPENIA;

EID: 0035865524     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V97.4.1147     Document Type: Article

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