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contentType Case Reports|Journal Article
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bibliographicCitation Bousfiha A, Bakhchane A, Charoute H, Detsouli M, Rouba H, Charif M, Lenaers G, Barakat A. Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family. Molecular Biology Reports. 2017 Sep 26;44(5):429–34. doi: 10.1007/s11033-017-4129-9.
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date 2017-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/28951997
https://doi.org/10.1007/s11033-017-4129-9
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language English
source https://scigraph.springernature.com/
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title Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family
discusses http://id.nlm.nih.gov/mesh/M0443139
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Total number of triples: 37.