Bernard-Soulier syndrome (Hemorrhagiparous thrombocytic dystrophy)

Orphanet Journal of Rare Diseases

Volumn 1, Issue 1, 2006, Pages

  Lanza, François ^a,b,c  

^a ETABLISSEMENT FRANÇAIS DU SANG   (France)

^b INSERM   (France)

^c UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

THROMBIN RECEPTOR;

BERNARD SOULIER DISEASE; GENETICS; HUMAN; MEGAKARYOCYTE; METABOLISM; MUTATION; PATHOLOGY; REVIEW; THROMBOCYTE; THROMBOCYTE COUNT;

BERNARD-SOULIER SYNDROME; BLOOD PLATELETS; HUMANS; MEGAKARYOCYTES; MUTATION; PLATELET COUNT; PLATELET GLYCOPROTEIN GPIB-IX COMPLEX;

EID: 33846606357     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-1-46     Document Type: Review

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