Matches in Nanopublications for { ?s ?p "[These findings strongly suggested that the I122V mutation in ACTG1 caused autosomal dominant non-syndromic hearing impairment in a Chinese family and expanded the spectrum of ACTG1 mutations causing hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP540303.RAXHyTDc5CDpl-BIRnKutlstDZvM0BNT3i-ePVLtSNSo8130_assertion description "[These findings strongly suggested that the I122V mutation in ACTG1 caused autosomal dominant non-syndromic hearing impairment in a Chinese family and expanded the spectrum of ACTG1 mutations causing hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540303.RAXHyTDc5CDpl-BIRnKutlstDZvM0BNT3i-ePVLtSNSo8130_provenance.
- NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_assertion description "[These findings strongly suggested that the I122V mutation in ACTG1 caused autosomal dominant non-syndromic hearing impairment in a Chinese family and expanded the spectrum of ACTG1 mutations causing hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- NP694059.RAREu_IbsbfMY1WBE2sowvX72Y9x1_QF-1h7ecSTxILq8130_assertion description "[These findings strongly suggested that the I122V mutation in ACTG1 caused autosomal dominant non-syndromic hearing impairment in a Chinese family and expanded the spectrum of ACTG1 mutations causing hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694059.RAREu_IbsbfMY1WBE2sowvX72Y9x1_QF-1h7ecSTxILq8130_provenance.