Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
about
Diagnosis of inherited bleeding disorders in the genomic era.Developmental Profiling of Tropomyosin Expression in Mouse Brain Reveals Tpm4.2 as the Major Post-synaptic Tropomyosin in the Mature Brain.On-target action of anti-tropomyosin drugs regulates glucose metabolism.ER/Golgi trafficking is facilitated by unbranched actin filaments containing Tpm4.2.Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia
P2860
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
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2017 nî lūn-bûn
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2017 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2017 թվականի հունվարին հրատարակված գիտական հոդված
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2017年の論文
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2017年論文
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2017年論文
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2017年論文
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2017年論文
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2017年論文
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2017年论文
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name
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
@ast
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
@en
type
label
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
@ast
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
@en
prefLabel
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
@ast
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
@en
P2093
P2860
P50
P356
P1476
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
@en
P2093
Andrew D Mumford
Chiara Lincetto
Christine A Lucas
Edna C Hardeman
Galina Schevzov
Irina Pleines
Joanne Woods
Kate Downes
Katja Aurbach
Marloes R Tijssen
P2860
P304
P356
10.1172/JCI86154
P407
P50
P577
2017-01-30T00:00:00Z