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Article

Fibrinogen Tokushima II: a new case of congenital dysfibrinogenemia with a γ methionine-310 to threonine substitution.

International journal of hematology - 1 Sept 2012

Shigekiyo Toshio, Sekimoto Etsuko, Shirakami Atsuhisa, Yamaguchi Hiroshi, Shibata Hironobu, Ozaki Shuji, Maegawa Masahiko, Aihara Ken-ichi

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Share to Afibrinogenemia
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22836217
DOI: 10.1007/s12185-012-1148-0

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Fibrinogen Tokushima II: a new case of congenital dysfibrinogenemia with a γ methionine-310 to threonine substitution.PMID 22836217Read ↗

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Human Fibrinogen: Molecular and Genetic Aspects of Congenital DisordersSemantic proximity Read ↗

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Fibrinogen Otsu I:A gammaAsn319,Asp320 deletion dysfibrinogen identified in an asymptomatic pregnant woman.Semantic proximity Read ↗

Fibrinogen Matsumoto II: gamma 308 Asn-->Lys (AAT-->AAG) mutation associated with bleeding tendency.Semantic proximity Read ↗

Fibrinogen Melbourne: a novel congenital hypodysfibrinogenemia caused by γ326Cys-Phe in the fibrinogen γ chain, presenting as massive splanchnic venous thrombosis.Semantic proximity Read ↗

One Hundred Years of Congenital Fibrinogen Disorders.Semantic proximity Read ↗

A novel γ-chain mutation p.Asp318His in a Chinese family with dysfibrinogenemia.Semantic proximity Read ↗

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Fibrinogen Leipzig II (gamma351Gly-->Ser and gamma82Ala-->Gly): hypodysfibrinogenaemia due to two independent amino acid substitutions within the same polypeptide chain.Semantic proximity Read ↗

Fibrinogen Kyoto II, a new congenitally abnormal molecule, characterized by the replacement of A alpha proline-18 by leucine.Semantic proximity Read ↗

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