Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

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Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

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2017年论文

@zh

2017年论文

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Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

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Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

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Item

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Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

@en

Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

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Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

@en

Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

@nl

P1476

Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.

@en

P2093

Omar Abdel-Wahab

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P2860

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome

Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA).

Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

Modulating splicing with small molecular inhibitors of the spliceosome

CryoEM structures of two spliceosomal complexes: starter and dessert at the spliceosome feast

Molecular Architecture of SF3b and Structural Consequences of Its Cancer-Related Mutations

Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts

P2888

s12185-017-2242-0

P304

720-731

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P31

scholarly article

P356

10.1007/S12185-017-2242-0

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P433

http://www.w3.org/2001/XMLSchema#string

P478

105

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P50

Akihide Yoshimi

P577

2017-05-02T00:00:00Z

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P698

28466384

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