Bernard-soulier syndrome due to compound heterozygosity for a novel glycoprotein ibβ mutation

Acta Haematologica

Volumn 131, Issue 1, 2013, Pages 46-49

  Sato, Tetsuji ^a   Kunishima, Shinji ^b   Shirayama, Rie ^a   Ichikawa, Shun ^a   Sakai, Michio ^a   Kusuhara, Koichi ^a  

^a UNIVERSITY OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH   (Japan)

^b NATIONAL HOSPITAL ORGANIZATION NAGOYA MEDICAL CENTER   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPROTEIN IB; GLYCOPROTEIN IB BETA; IMMUNOGLOBULIN; UNCLASSIFIED DRUG; GLYCOCALICIN; GLYCOPROTEIN 1B BETA;

ARTICLE; BERNARD SOULIER DISEASE; BLEEDING TENDENCY; BLOOD EXAMINATION; CASE REPORT; FEMALE; HETEROZYGOSITY; HUMAN; NEONATAL ALLOIMMUNE THROMBOCYTOPENIA; NEWBORN; PRIORITY JOURNAL; THROMBOCYTE AGGREGATION; THROMBOCYTE COUNT; THROMBOCYTOPENIA; VEIN PUNCTURE; BIRTH WEIGHT; BLOOD SMEAR; FLOW CYTOMETRY; GENE MUTATION; GESTATIONAL AGE; HOMOZYGOSITY; HOSPITALIZATION; IMMUNOBLOTTING; LIMIT OF DETECTION; MISSENSE MUTATION;

BERNARD-SOULIER SYNDROME; BLOOD PLATELETS; FEMALE; HETEROZYGOTE; HUMANS; MUTATION; PLATELET GLYCOPROTEIN GPIB-IX COMPLEX;

EID: 84890897671     PISSN: 00015792     EISSN: 14219662     Source Type: Journal    
DOI: 10.1159/000351057     Document Type: Article

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