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Catalogue record is a nonfiction available to read on EtoBox.
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Syndromic Hearing Loss in Moroccan families is associated to homozygous missense variants in COL4A3 and MASP1 1 1 Introduction 1 2 Patients and methods 3 2.1 Patients 3 2.2 Genetic analyses 3 2.3 Molecular modelling and stability analysis 3 3 Results 3 3.1 Identification of the pathogenic variants 3 3.2 Co-segregation analysis 3 3.3 Molecular modelling and stability analysis 3 4 Discussion 4 5 Conclusion 4 Data availability statement 4 Ethical approval 4 CRediT authorship contribution statement 4 Declaration of Competing Interest 4 Acknowledgements 4 References 5
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Common subject areas: history, science, philosophy, social sciences.
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