Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population.Clinical Consequences and Molecular Bases of Low Fibrinogen Levels.

P2860

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P2860

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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http://www.wikidata.org/entity/Q45886377

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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name

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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type

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Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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prefLabel

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

@en

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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P1476

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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A Srivastava

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A Viswabandya

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B George

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E Sumitha

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G R Jayandharan

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G S Devi

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M Chandy

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N Arora

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P Shenbagapriya

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S C Nair

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P2860

Fibrinogen

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion

Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations

Human non-synonymous SNPs: server and survey

Prediction of deleterious human alleles

Bernard-Soulier syndrome due to the homozygous Asn-45Ser mutation in GPIX: an unexpected, frequent finding in Germany.

Towards a structural basis of human non-synonymous single nucleotide polymorphisms.

Recessively inherited coagulation disorders.

Fibrinogen and fibrin structure and functions.

The molecular basis of quantitative fibrinogen disorders.

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611-618

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scholarly article

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10.1111/HAE.12143

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Aby Abraham

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2013-04-08T00:00:00Z

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India

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

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P2860

P2860

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

description

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

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P577

P698

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P1433

P1476

P2093

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P478

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P577

P698

P921