reference/27470884

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/27470884

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publicationName	Journal of thrombosis and haemostasis : JTH
startingPage	1482
bibliographicCitation	JAYANDHARAN G, VISWABANDYA A, BAIDYA S, NAIR SC, SHAJI RV, GEORGE B, CHANDY M, SRIVASTAVA A. Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T→G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin. Journal of Thrombosis and Haemostasis. 2005 Jul;3(7):1482–7. doi: 10.1111/j.1538-7836.2005.01339.x.
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date	200507
identifier	https://pubmed.ncbi.nlm.nih.gov/15892863 https://doi.org/10.1111/j.1538-7836.2005.01339.x
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language	English
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title	Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin
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Total number of triples: 68.