Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
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Clinical Consequences and Molecular Bases of Low Fibrinogen Levels.Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.Comparative omics and feeding manipulations in chicken indicate a shift of the endocrine role of visceral fat towards reproduction.Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders
P2860
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
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2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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name
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
@en
type
label
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
@en
prefLabel
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
@en
P2093
P2860
P50
P356
P1433
P1476
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia
@en
P2093
K Devreese
P de Moerloose
V Mondelaers
Y Beauverd
P2860
P304
P356
10.1111/HAE.13190
P577
2017-03-17T00:00:00Z