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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 2 |
2015 | 1 |
2019 | 2 |
2024 | 0 |
PubMed for id: 436997
5 results
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Page 1
Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment.
Arch Iran Med. 2019 Apr 1;22(4):189-197.
Arch Iran Med. 2019.
PMID: 31126177
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing loss.
Ramzan M, Idrees H, Mujtaba G, Sobreira N, Witmer PD, Naz S.
Ramzan M, et al.
Gene. 2019 Jul 15;705:109-112. doi: 10.1016/j.gene.2019.04.064. Epub 2019 Apr 24.
Gene. 2019.
PMID: 31028865
Free PMC article.
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A novel frameshift mutation in KCNQ4 in a family with autosomal recessive non-syndromic hearing loss.
Wasano K, Mutai H, Obuchi C, Masuda S, Matsunaga T.
Wasano K, et al.
Biochem Biophys Res Commun. 2015 Aug 7;463(4):582-6. doi: 10.1016/j.bbrc.2015.05.099. Epub 2015 May 31.
Biochem Biophys Res Commun. 2015.
PMID: 26036578
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Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL.
Abdelfatah N, McComiskey DA, Doucette L, Griffin A, Moore SJ, Negrijn C, Hodgkinson KA, King JJ, Larijani M, Houston J, Stanton SG, Young TL.
Abdelfatah N, et al.
Eur J Hum Genet. 2013 Oct;21(10):1112-9. doi: 10.1038/ejhg.2013.5. Epub 2013 Feb 27.
Eur J Hum Genet. 2013.
PMID: 23443030
Free PMC article.
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Impaired surface expression and conductance of the KCNQ4 channel lead to sensorineural hearing loss.
Gao Y, Yechikov S, Vázquez AE, Chen D, Nie L.
Gao Y, et al.
J Cell Mol Med. 2013 Jul;17(7):889-900. doi: 10.1111/jcmm.12080. Epub 2013 Jun 11.
J Cell Mol Med. 2013.
PMID: 23750663
Free PMC article.
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