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Year | Number of Results |
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2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 1 |
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PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss.
Hum Genet. 2024 Mar;143(3):311-329. doi: 10.1007/s00439-024-02649-2. Epub 2024 Mar 9.
Hum Genet. 2024.
PMID: 38459354
Free PMC article.
PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss.
Redfield SE, De-la-Torre P, Zamani M, Wang H, Khan H, Morris T, Shariati G, Karimi M, Kenna MA, Seo GH, Xu H, Lu W, Naz S, Galehdari H, Indzhykulian AA, Shearer AE, Vona B.
Redfield SE, et al.
medRxiv [Preprint]. 2023 Dec 19:2023.10.08.23296081. doi: 10.1101/2023.10.08.23296081.
medRxiv. 2023.
PMID: 37873491
Free PMC article.
Updated.
Preprint.
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Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients.
Benson J, Stewart C, Kenna MA, Shearer AE.
Benson J, et al.
Laryngoscope. 2023 Jun;133(6):1501-1506. doi: 10.1002/lary.30350. Epub 2022 Aug 18.
Laryngoscope. 2023.
PMID: 37158261
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Dual-vector gene therapy restores cochlear amplification and auditory sensitivity in a mouse model of DFNB16 hearing loss.
Shubina-Oleinik O, Nist-Lund C, French C, Rockowitz S, Shearer AE, Holt JR.
Shubina-Oleinik O, et al.
Sci Adv. 2021 Dec 17;7(51):eabi7629. doi: 10.1126/sciadv.abi7629. Epub 2021 Dec 15.
Sci Adv. 2021.
PMID: 34910522
Free PMC article.
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