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Keyword [G mutation]
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1. Association Of +292C/G Mutation At Promoter Of Human Urate Transporter 1 Gene And Primary Hyperuricemia
2. Mutation Maps Drawing And Analysis Of Common Deafness Genes Among Non-syndromic Hearing Loss In Northwest China
3. Molecular Mechanism On The Mitochondrial TRNAAsp 7551A>G Mutation Associated With Deafness
4. Analysis Of Disease Gene Mutation And Function In A Patient With Axenfeld-Rieger Syndrome
5. Relationship Between The Mitochondrial DNA12026A→G Mutation And Diabetic Nephropathy In Yanbian Population
6. The Clinical And Genetic Analysis Of Heteroplasmic 3243A>G Mutation In Mitochondrial TRNALeu（UUR） Gene Among 6 Chinese Patients With MELAS
7. Mitochondrial Functional Study Associated With M.1555A>G Mutation Based On Deaf-Specific Induced Pluripotent Stem Cells
8. Risk Analysis Of Diabetes Based On Family History And The Screening Of The Mt3243A>G Mutation In Community-based Diabetic Patients
9. Clinical Phenotypes And Mitochondrial And Cell Biomechanical Function Of The M.3243A>G Mutation
10. The Clinical And Molecular Research Of Mitochondrial Inherited Deafness And Nuclear Modified Genes
11. Development Of Therapeutic Anusense Oligonucleotides To Treat Hearing Loss Caused By SLC26A4 C.919-2A>G Mutation
12. Phenotype Of A Mouse Model Of Combined Methylmalonic Acidemia Caused By MMACHC Gene C.80A>G(p.G27R) Homozygous Mutation
13. Clinical Characteristics Of Patients With Early-onset Diabetes In Yangzhou Area
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