Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigmentosa

Overview of attention for article published in BMC Ophthalmology, November 2022

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High Attention Score compared to outputs of the same age and source (84th percentile)

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twitter: 2 X users

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So far, Altmetric has seen 4 X posts from 2 X users, with an upper bound of 2,541 followers.

RT @WaltherCancerIn: @TomSChangMD "Here we present a case of Usher syndrome type 1F (USH1F) with a novel homozygous variant in the calcium-…

28 Oct 2023

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@TomSChangMD "Here we present a case of Usher syndrome type 1F (USH1F) with a novel homozygous variant in the calcium-dependent cell-cell adhesion protocadherin-15 (PCDH15) gene" https://t.co/WhekOpLWmp

28 Oct 2023

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RT @TomSChangMD: Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigme…

28 Oct 2023

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Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigmentosa https://t.co/s6wBCkNhAW #Ophthalmology #Eyecare #Health #Healthcare #Medical #Doctor #Doctors #MD

17 Nov 2022

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