Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia.

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Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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Heterozygous Mutations in OAS1 ...... is with Hypogammaglobulinemia.

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Heterozygous Mutations in OAS1 ...... is with Hypogammaglobulinemia.

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Heterozygous Mutations in OAS1 ...... is with Hypogammaglobulinemia.

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Heterozygous Mutations in OAS1 ...... is with Hypogammaglobulinemia.

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Heterozygous Mutations in OAS1 ...... is with Hypogammaglobulinemia.

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Heterozygous Mutations in OAS1 ...... is with Hypogammaglobulinemia.

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P1476

Heterozygous Mutations in OAS1 ...... is with Hypogammaglobulinemia.

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P2093

Atsushi Fujita

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Hirokazu Kanegane

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Hisanori Minakami

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Itaru Hayasaka

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Kazuhiro Ogata

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Kazunaga Agematsu

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Kazutoshi Cho

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Koh Nakata

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Mari Tanaka-Kubota

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Masaaki Shiina

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P2860

Structural basis for cytosolic double-stranded RNA surveillance by human oligoadenylate synthetase 1

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Crystal structure of the 2'-specific and double-stranded RNA-activated interferon-induced antiviral protein 2'-5'-oligoadenylate synthetase

A mutation in the surfactant protein C gene associated with familial interstitial lung disease

Association of SARS susceptibility with single nucleic acid polymorphisms of OAS1 and MxA genes: a case-control study.

A graphical interface for the FoldX forcefield.

Gene structure and function of the 2'-5'-oligoadenylate synthetase family.

Standardized serum GM-CSF autoantibody testing for the routine clinical diagnosis of autoimmune pulmonary alveolar proteinosis.

Genotype-phenotype correlations for infants and children with ABCA3 deficiency

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scholarly article

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10.1016/J.AJHG.2018.01.019

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English

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2018-02-12T00:00:00Z

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29455859

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5985284

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