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V. shenbagapriya
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V. Shenbaga Priya
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Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation.
Thromb Haemost. 2011 Jun;105(6):1120-3. doi: 10.1160/TH10-11-0767. Epub 2011 Apr 20.
Thromb Haemost. 2011.
PMID: 21647534
No abstract available.
Molecular basis of Bernard-Soulier syndrome in 27 patients from India.
Sumitha E, Jayandharan GR, David S, Jacob RR, Sankari Devi G, Bargavi B, Shenbagapriya S, Nair SC, Abraham A, George B, Viswabandya A, Mathews V, Chandy M, Srivastava A.
Sumitha E, et al.
J Thromb Haemost. 2011 Aug;9(8):1590-8. doi: 10.1111/j.1538-7836.2011.04417.x.
J Thromb Haemost. 2011.
PMID: 21699652
Free article.
BACKGROUND: Bernard-Soulier syndrome (BSS) is an extremely rare (1:1 million) bleeding disorder of platelet adhesion, caused by defects in the glycoprotein (GP)Ib/IX/V complex. PATIENTS AND METHODS: The diagnosis in 27 patients was based on low platelet count, presence of …
BACKGROUND: Bernard-Soulier syndrome (BSS) is an extremely rare (1:1 million) bleeding disorder of platelet adhesion, caused by defects in t …
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