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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2003 | 1 |
2009 | 1 |
2010 | 2 |
2024 | 0 |
PubMed (cited) for id: 613391
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Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction.
Am J Hum Genet. 2010 Apr 9;86(4):604-10. doi: 10.1016/j.ajhg.2010.02.015. Epub 2010 Mar 25.
Am J Hum Genet. 2010.
PMID: 20346435
Free PMC article.
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
Shahin H, Walsh T, Rayyan AA, Lee MK, Higgins J, Dickel D, Lewis K, Thompson J, Baker C, Nord AS, Stray S, Gurwitz D, Avraham KB, King MC, Kanaan M.
Shahin H, et al.
Eur J Hum Genet. 2010 Apr;18(4):407-13. doi: 10.1038/ejhg.2009.190. Epub 2009 Nov 4.
Eur J Hum Genet. 2010.
PMID: 19888295
Free PMC article.
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A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles.
Goodyear RJ, Legan PK, Wright MB, Marcotti W, Oganesian A, Coats SA, Booth CJ, Kros CJ, Seifert RA, Bowen-Pope DF, Richardson GP.
Goodyear RJ, et al.
J Neurosci. 2003 Oct 8;23(27):9208-19. doi: 10.1523/JNEUROSCI.23-27-09208.2003.
J Neurosci. 2003.
PMID: 14534255
Free PMC article.
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