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Genotype Characterization and MiRNA Expression Profiling in Usher Syndrome Cell Lines

Sep 28, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me Int J Mol Sci. 2024 Sep 17;25(18):9993. doi: 10.3390/ijms25189993.ABSTRACTUsher syndrome (USH) is an inherited disorder characterized by sensorineural hearing loss (SNHL),...

A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family

Sep 20, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me Orphanet J Rare Dis. 2024 Sep 20;19(1):349. doi: 10.1186/s13023-024-03348-x.ABSTRACTBACKGROUND: Usher syndrome type 3 (USH3) is an autosomal recessive inherited disorder caused...

Censoring the Floor Effect in Long-Term Stargardt Disease Microperimetry Data Produces a Faster Rate of Decline

Sep 16, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me Ophthalmol Sci. 2024 Jul 20;4(6):100581. doi: 10.1016/j.xops.2024.100581. eCollection 2024 Nov-Dec.ABSTRACTPURPOSE: To evaluate progression rate estimation in long-term Stargardt...

Genotype Characterization and MiRNA Expression Profiling in Usher Syndrome Cell Lines

A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family

Censoring the Floor Effect in Long-Term Stargardt Disease Microperimetry Data Produces a Faster Rate of Decline

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