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.
about
Diffuse large B cell lymphoma in wiskott-Aldrich syndrome: a case report and review of literatureMolecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.Haematology research in India: past, present and future.Unexplained discrepancies in the activity--antigen ratio in congenital FX deficiencies with defects in the catalytic domain.Recurrence of a Phe31Ser mutation in the Gla domain of blood coagulation factor X, in unrelated Algerian families: a founder effect?Hemostasis research in India: past, present, and future.Genetic analysis of bleeding disorders.The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain.Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India.Molecular basis of quantitative fibrinogen disorders in 27 patients from India.Molecular basis of Bernard-Soulier syndrome in 27 patients from India.
P2860
Q33418318-AF1EC73E-B62F-4523-A8F9-6156D2AEB311Q34282200-15ABCB47-B442-40E2-92BC-DC715CA25FB5Q35106402-A0345D4E-AA04-484C-95AF-FCCFAD67E79BQ37576865-3A843602-8639-42C2-ACF2-527F75E2EAC0Q38865031-3A20AFDA-6E06-4905-B02F-46A1B95E791AQ39022458-DA4FBFC4-F81D-46E2-86F2-B8A5446AE3B5Q40616276-20248106-B123-4F71-9EFB-D1F295965A00Q43485191-75156932-F6FE-42BD-A750-BC1DDA2CF3EAQ45876213-53F12EDD-0D2B-40FF-B3F9-4B17A8A4D392Q45886377-B19BE85D-E658-47D9-AC56-3C201744EF6EQ54363282-C93F3264-1CD2-4E75-88EA-F3B447C94FB8
P2860
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.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Six novel mutations including ...... s of Nepali and Indian origin.
@en
type
label
Six novel mutations including ...... s of Nepali and Indian origin.
@en
prefLabel
Six novel mutations including ...... s of Nepali and Indian origin.
@en
P2093
P2860
P1476
Six novel mutations including ...... s of Nepali and Indian origin.
@en
P2093
Jayandharan G
Srivastava A
Viswabandya A
P2860
P304
P356
10.1111/J.1538-7836.2005.01339.X
P577
2005-05-09T00:00:00Z