A candidate gene for autoimmune myasthenia gravis. - Wikidata - awgldk - TriplyDB

A candidate gene for autoimmune myasthenia gravis.

A candidate gene for autoimmune myasthenia gravis.

http://www.wikidata.org/entity/Q34284842

about

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12 Functional defect in regulatory T cells in myasthenia gravis.Rheumatoid Arthritis in Latin Americans Enriched for Amerindian Ancestry Is Associated With Loci in Chromosomes 1, 12, and 13, and the HLA Class II Region

P2860

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P2860

A candidate gene for autoimmune myasthenia gravis.

http://www.wikidata.org/entity/Q34284842

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

A candidate gene for autoimmune myasthenia gravis.

@ast

A candidate gene for autoimmune myasthenia gravis.

@en

A candidate gene for autoimmune myasthenia gravis.

@nl

type

label

A candidate gene for autoimmune myasthenia gravis.

@ast

A candidate gene for autoimmune myasthenia gravis.

@en

A candidate gene for autoimmune myasthenia gravis.

@nl

prefLabel

A candidate gene for autoimmune myasthenia gravis.

@ast

A candidate gene for autoimmune myasthenia gravis.

@en

A candidate gene for autoimmune myasthenia gravis.

@nl

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P1476

A candidate gene for autoimmune myasthenia gravis.

@en

P2093

Abdel Elkahloun

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

Addis A Taye

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

Barrington G Burnett

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

Bryan J Traynor

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

Carlo Rinaldi

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

Dena Hernandez

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

Guida Landouré

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

Horia Stanescu

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

Janel O Johnson

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

Kenneth H Fischbeck

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

P2860

Molecular cloning and characterization of a tumor-associated, growth-related, and time-keeping hydroquinone (NADH) oxidase (tNOX) of the HeLa cell surface

New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome

A mosaic activating mutation in AKT1 associated with the Proteus syndrome

Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations

High sensitivity of CD4+CD25+ regulatory T cells to extracellular metabolites nicotinamide adenine dinucleotide and ATP: a role for P2X7 receptors

Parametric and nonparametric linkage analysis: a unified multipoint approach

Micro RNAs are complementary to 3' UTR sequence motifs that mediate negative post-transcriptional regulation

Familial autoimmune myasthenia gravis: report of four families.

Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing.

Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis.

P304

342-347

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scholarly article

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10.1212/WNL.0B013E318260CBD0

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P407

P433

4

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P478

79

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Leslie G Biesecker

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2012-06-27T00:00:00Z

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P5875

228088543

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22744667

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myasthenia gravis

P932

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