Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility

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Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility

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im August 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в серпні 2018

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Homozygous loss-of-function mu ...... ts and likely male infertility

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Homozygous loss-of-function mu ...... ts and likely male infertility

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Homozygous loss-of-function mu ...... ts and likely male infertility

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Homozygous loss-of-function mu ...... ts and likely male infertility

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Homozygous loss-of-function mu ...... ts and likely male infertility

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Homozygous loss-of-function mu ...... ts and likely male infertility

@nl

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Homozygous loss-of-function mu ...... ts and likely male infertility

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Alaa Darwish

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Alper Gezdirici

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Avraham Shaag

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Azaria J J T Rein

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Christine Edelbusch

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Dinu Antony

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Dorus A Mans

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Elif Yilmaz Gulec

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Friederike Stuhlmann

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Gerard W Dougherty

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Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia

CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation

Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia

Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia

MNS1 is essential for spermiogenesis and motile ciliary functions in mice

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e1007602

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scholarly article

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10.1371/JOURNAL.PGEN.1007602

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English

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P478

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P577

2018-08-27T00:00:00Z

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30148830

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P921

cancer research

molecular biology

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6128653

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