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issn 2324-9269
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publicationName Molecular Genetics & Genomic Medicine
startingPage e1866
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bibliographicCitation Bharadwaj T, Schrauwen I, Acharya A, Nouel-Saied LM, Väisänen ML, Kraatari M, Rahikkala E, Jarvela I, Kotimäki J, Leal SM. Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. Mol Genet Genomic Med. 2022 Mar;10(3):e1866. PMID: 35150090; PMCID: PMC8922966.
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date 2022-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language English
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title Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant
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Total number of triples: 40.