Distribution of ELOVL4 in the Developing and Adult Mouse Brain. - Wikidata - awgldk - TriplyDB

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

http://www.wikidata.org/entity/Q33619349

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Homozygous Expression of Mutant ELOVL4 Leads to Seizures and Death in a Novel Animal Model of Very Long-Chain Fatty Acid Deficiency.

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P2860

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

http://www.wikidata.org/entity/Q33619349

description

2017 nî lūn-bûn

@nan

2017 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի մայիսին հրատարակված գիտական հոդված

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2017年の論文

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2017年論文

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2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

name

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

@ast

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

@en

type

label

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

@ast

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

@en

prefLabel

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

@ast

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

@en

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FNANA.2017.00038

P1433

Frontiers in Neuroanatomy

P1476

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

@en

P2093

Blake R Hopiavuori

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

David M Sherry

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

Ferenc Deak

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

Kathryn G Ozan

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Martin-Paul Agbaga

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

Megan A Stiles

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

Negar S Rahman

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

Robert E Anderson

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

P2860

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy

Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia

Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4

Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4

Genome-wide atlas of gene expression in the adult mouse brain

A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family

DSPP mutation in dentinogenesis imperfecta Shields type II

Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein

NeuN, a neuronal specific nuclear protein in vertebrates

Role of Stargardt-3 macular dystrophy protein (ELOVL4) in the biosynthesis of very long chain fatty acids

P304

38

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P31

scholarly article

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10.3389/FNANA.2017.00038

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11

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2017-05-01T00:00:00Z

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28507511

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P932

5410580

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