Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract.

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The role of Eph receptors in lens function and disease Corneal aldehyde dehydrogenases: multiple functions and novel nuclear localization Association of the ephreceptor tyrosinekinase-type A2 (EPHA2) gene polymorphism rs3754334 with age-related cataract risk: a meta-analysis.

P2860

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P2860

Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract.

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http://www.wikidata.org/entity/Q36926704

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2008 nî lūn-bûn

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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name

Investigation of eight candida ...... ant total congenital cataract.

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Investigation of eight candida ...... ant total congenital cataract.

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Investigation of eight candida ...... ant total congenital cataract.

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P1476

Investigation of eight candida ...... nant total congenital cataract

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P2093

David A Mackey

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Jamie E Craig

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Kate J Laurie

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Kathryn Hattersley

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Richard L Maas

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Salil A Lachke

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P2860

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy

A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2

Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2

Actin binding proteins: regulation of cytoskeletal microfilaments

Transcription factor MIZ-1 is regulated via microtubule association

ESEfinder: A web resource to identify exonic splicing enhancers

Alteration in the ubiquitin structure and function in the human lens: a possible mechanism of senile cataractogenesis.

An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers.

Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans

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1799-1804

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scholarly article

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Kathryn P. Burdon

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2008-09-30T00:00:00Z

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18843385

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birth defect

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2563027

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Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract.

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P2860

P2860

Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract.

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P1476

P2093

P2860

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