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Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis

Overview of attention for article published in Frontiers in Neuroscience, August 2018
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Title
Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
Published in
Frontiers in Neuroscience, August 2018
DOI 10.3389/fnins.2018.00570
Pubmed ID
Authors

Yan Lu, Yu-Wei Da, Yong-Biao Zhang, Xin-Gang Li, Min Wang, Li Di, Mi Pang, Lin Lei

Abstract

[This corrects the article DOI: 10.3389/fnins.2018.00329.].

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Geographical breakdown

Country Count As %
Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 1 100%
Readers by discipline Count As %
Medicine and Dentistry 1 100%