Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference30 articles.
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2. Mitochondrial dysfunction as a cause of optic neuropathies;Carelli;Prog Retin Eye Res,2004
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4. Prevalence of mitochondrial DNA disease in adults;Schaefer;Ann Neurol,2008
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1. Rapid and Sensitive Diagnosis of Leber Hereditary Optic Neuropathy Variants Using CRISPR/Cas12a Detection;The Journal of Molecular Diagnostics;2023-08
2. GenEye24: Novel rapid screening test for the top-3 Leber’s Hereditary Optic Neuropathy pathogenic sequence variants;Mitochondrion;2023-03
3. Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method;Bioscience Reports;2020-05
4. Three Cases of Leber’s Hereditary Optic Neuropathy with Rapid Increase in Visual Acuity After Gene Therapy;Current Gene Therapy;2019-08-20
5. Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers;BMC Research Notes;2018-12
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