DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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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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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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P1476

DNA recombination defects in Kuwait: Clinical, immunologic and genetic profile.

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P2093

Janet Chou

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Luigi D Notarangelo

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Michel J Massaad

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Raif S Geha

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Waleed Al-Herz

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P2860

Fast and accurate short read alignment with Burrows-Wheeler transform

Human RAG mutations: biochemistry and clinical implications

A framework for variation discovery and genotyping using next-generation DNA sequencing data

Crystal structure of the V(D)J recombinase RAG1-RAG2

Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia

A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans.

Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow.

Transplantation outcomes for severe combined immunodeficiency, 2000-2009.

PTIP associates with Artemis to dictate DNA repair pathway choice.

The long quest for neonatal screening for severe combined immunodeficiency.

P31

scholarly article

P356

10.1016/J.CLIM.2017.10.006

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P577

2017-10-16T00:00:00Z

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P698

29051008

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P932

5826831

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