Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

about

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

Item

http://www.wikidata.org/entity/Q47687617

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

@en

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

@nl

type

Item

label

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

@en

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

@nl

prefLabel

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

@en

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

@nl

P1476

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

@en

P2093

Adam P DeLuca

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

Alan L Robin

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

Jeffrey Liebmann

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

Kazuhide Kawase

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

Robert Ritch

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

P2860

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma

Fast and accurate short read alignment with Burrows-Wheeler transform

Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing

The number of people with glaucoma worldwide in 2010 and 2020

Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma

Molecular cloning, genomic structure, and protein characterization of mouse optineurin

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

Copy number variation detection and genotyping from exome sequence data.

GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.

P304

1063-1067

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

P31

scholarly article

P356

10.1097/IJG.0000000000000792

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

P433

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

P478

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

P50

P577

2017-09-03T00:00:00Z

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

P698

28984711

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

P932

5716909

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