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issn 1755-8794
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publicationName BMC Medical Genomics
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bibliographicCitation Rayat S, Farhadi M, Emamdjomeh H, Morovvati S, Falah M. Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness. BMC Medical Genomics. 2022 Jun 16;15(1):133. doi: 10.1186/s12920-022-01287-9.
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date 2022-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1186/s12920-022-01287-9
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language English
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title Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness
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Total number of triples: 31.