Compound Heterozygous Variants in the Coiled-Coil Domain Containing 40 Gene in a Chinese Family with Primary Ciliary Dyskinesia Cause Extreme Phenotypic Diversity in Cilia Ultrastructure.

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Corrigendum: Compound Heterozygous Variants in the Coiled-Coil Domain Containing 40 Gene in a Chinese Family With Primary Ciliary Dyskinesia Cause Extreme Phenotypic Diversity in Cilia Ultrastructure.

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Q55223136-249A115A-D3ED-4328-9EEB-4C4283B2F589

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Compound Heterozygous Variants in the Coiled-Coil Domain Containing 40 Gene in a Chinese Family with Primary Ciliary Dyskinesia Cause Extreme Phenotypic Diversity in Cilia Ultrastructure.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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name

Compound Heterozygous Variants ...... rsity in Cilia Ultrastructure.

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Compound Heterozygous Variants ...... rsity in Cilia Ultrastructure.

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Compound Heterozygous Variants ...... rsity in Cilia Ultrastructure.

@en

Compound Heterozygous Variants ...... rsity in Cilia Ultrastructure.

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Compound Heterozygous Variants ...... rsity in Cilia Ultrastructure.

@en

Compound Heterozygous Variants ...... rsity in Cilia Ultrastructure.

@nl

P1476

Compound Heterozygous Variants ...... rsity in Cilia Ultrastructure.

@en

P2093

Haixia Chen

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

Hui Huang

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

Jie Cao

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

Jing Wu

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

Lin Yang

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

Na Yi

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

Peng Han

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

Santasree Banerjee

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

Shunyu Feng

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

Xiaohong Bai

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

P2507

P2860

Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

The axoneme: the propulsive engine of spermatozoa and cilia and associated ciliopathies leading to infertility

Overview of structure and function of mammalian cilia

The dynein regulatory complex is the nexin link and a major regulatory node in cilia and flagella.

Atg7 is required for acrosome biogenesis during spermatogenesis in mice

Primary ciliary dyskinesia (PCD).

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Pregnancy after ICSI with ejaculated immotile spermatozoa from a patient with immotile cilia syndrome: a case report and review of the literature.

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scholarly article

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10.3389/FGENE.2018.00023

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2018-02-02T00:00:00Z

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29456554

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P921

dyskinesia

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5801289

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Compound Heterozygous Variants in the Coiled-Coil Domain Containing 40 Gene in a Chinese Family with Primary Ciliary Dyskinesia Cause Extreme Phenotypic Diversity in Cilia Ultrastructure.

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P921

P921

Compound Heterozygous Variants in the Coiled-Coil Domain Containing 40 Gene in a Chinese Family with Primary Ciliary Dyskinesia Cause Extreme Phenotypic Diversity in Cilia Ultrastructure.

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P1433

P1476

P2093

P2507

P2860

P304

P31

P356

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2507

P2860

P304

P31

P356

P478

P577

P698

P921

P932