Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study - Wikidata - wikimedia - TriplyDB

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

http://www.wikidata.org/entity/Q33503411

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The current research status of normal tension glaucoma VAV2 and VAV3 as candidate disease genes for spontaneous glaucoma in mice and humans Mitochondrial disorders and the eye.Glaucoma: genes, phenotypes, and new directions for therapy.Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.Association of OPA1 polymorphisms with NTG and HTG: a meta-analysis.Mitochondrial genome analysis of primary open angle glaucoma patients Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy Association of SOD2 polymorphisms with primary open angle glaucoma in a Chinese population.Association of Mn-SOD mutation (c.47T > C) with various POAG clinical indices.

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Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

http://www.wikidata.org/entity/Q33503411

description

2009 nî lūn-bûn

@nan

2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Evaluation of nine candidate g ...... glaucoma: a case control study

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Evaluation of nine candidate g ...... glaucoma: a case control study

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Evaluation of nine candidate g ...... glaucoma: a case control study

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Evaluation of nine candidate g ...... glaucoma: a case control study

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Evaluation of nine candidate g ...... glaucoma: a case control study

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Evaluation of nine candidate g ...... glaucoma: a case control study

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1471-2350-10-91

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BMC Medical Genetics

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Evaluation of nine candidate g ...... glaucoma: a case control study

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Bernd Wissinger

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Christiane Wolf

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Eugen Gramer

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Eva Reinthal

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Francesca Pasutto

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Nicole Weisschuh

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P2860

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21

Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma

OPA1 requires mitofusin 1 to promote mitochondrial fusion

PLINK: a tool set for whole-genome association and population-based linkage analyses

The number of people with glaucoma worldwide in 2010 and 2020

The structure of haplotype blocks in the human genome

The International HapMap Project

Haploview: analysis and visualization of LD and haplotype maps

The association between Japanese primary open-angle glaucoma and normal tension glaucoma patients and the optineurin gene

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1471-2350-10-91

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10.1186/1471-2350-10-91

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10

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Bertram Müller-Myhsok

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2009-09-15T00:00:00Z

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26812796

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