The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient
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Title
The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient
Authors
Keywords
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Journal
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2021-01-06
DOI
10.1007/s10815-020-02036-6
References
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- (2018) Adam J. Shapiro et al. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
- Genetics of male infertility
- (2018) Csilla Krausz et al. Nature Reviews Urology
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- (2018) Kyeong Jee Cho et al. PLoS Genetics
- Whole-Exome Sequencing Identified a Novel Compound Heterozygous Mutation of LRRC6 in a Chinese Primary Ciliary Dyskinesia Patient
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- European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia
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- Diagnostic Methods in Primary Ciliary Dyskinesia
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- (2014) Johanna Raidt et al. EUROPEAN RESPIRATORY JOURNAL
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- Loss-of-Function Mutations in LRRC6 , a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms, Cause Primary Ciliary Dyskinesia
- (2012) Esther Kott et al. AMERICAN JOURNAL OF HUMAN GENETICS
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