Case of Cone Dystrophy with Normal Fundus Appearance Associated with Biallelic POC1B Variants.

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Case of Cone Dystrophy with Normal Fundus Appearance Associated with Biallelic POC1B Variants.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Case of Cone Dystrophy with No ...... with Biallelic POC1B Variants.

@en

Case of Cone Dystrophy with No ...... with Biallelic POC1B Variants.

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type

Item

label

Case of Cone Dystrophy with No ...... with Biallelic POC1B Variants.

@en

Case of Cone Dystrophy with No ...... with Biallelic POC1B Variants.

@nl

prefLabel

Case of Cone Dystrophy with No ...... with Biallelic POC1B Variants.

@en

Case of Cone Dystrophy with No ...... with Biallelic POC1B Variants.

@nl

P1476

Case of Cone Dystrophy with No ...... with Biallelic POC1B Variants.

@en

P2093

Ayami Nakanishi

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Azusa Kominami

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Hiroko Terasaki

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Kaoru Fujinami

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Kazushige Tsunoda

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Sachiko Kikuchi

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Shinji Ueno

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Shuhei Kameya

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Takaaki Hayashi

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Takeshi Iwata

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P2860

Poc1A and Poc1B act together in human cells to ensure centriole integrity

Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy

Mutation of POC1B in a severe syndromic retinal ciliopathy

A highly conserved Poc1 protein characterized in embryos of the hydrozoan Clytia hemisphaerica: localization and functional studies

In vivo imaging of human cone photoreceptor inner segments.

Human photoreceptor topography.

NEAR-INFRARED REFLECTANCE IMAGING IN EYES WITH ACUTE ZONAL OCCULT OUTER RETINOPATHY.

New Tetrahymena basal body protein components identify basal body domain structure.

Molecular architecture of the centriole proteome: the conserved WD40 domain protein POC1 is required for centriole duplication and length control.

Retinal structure and function in achromatopsia: implications for gene therapy.

P304

1-8

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P31

scholarly article

P356

10.1080/13816810.2017.1408846

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P577

2017-12-08T00:00:00Z

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P698

29220607

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