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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Disease Progression and USH2A[original query]
Clinical and Haplotypic Variability of Slovenian USH2A Patients Homozygous for the c. 11864G>A Nonsense Mutation.
Genes 2019 12 10 (12): .
Zupan Andrej, Fakin Ana, Battelino Saba, Jarc-Vidmar Martina, Hawlina Marko, Bonnet Crystel, Petit Christine, Glava? Damj
High prevalence of exon-13 variants in USH2A-related retinal dystrophies in Taiwanese population.
Orphanet journal of rare diseases 2024 6 19 (1): 238.
Yu-Wei Lin, Yu-Shu Huang, Chien-Yu Lin, Chao-Wen Lin, Chen-Chi Wu, Chang-Hao Yang, Chung-May Yang, Pei-Lung Chen, Ta-Ching Ch
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