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Keyword [nuclear modifier gene]
Result: 1 - 3 | Page: 1 of 1
1.
Molecular Pathogenesis Study For An Extensive Nonsyndomic Deafness Family Associated With A1555G Mutation
2.
Sequence Analysis Of The Complete Mitochondrial Genome And TRMU Gene Of Two Pedigrees With Hearing Impairment Associated With The 12S RRNA A827G Mutation
3.
Nuclear Modifier Gene PRICKLE3 Manifests The Tissue-specific Defects Of Retinal Ganglion Cells Bearing LHON-associated MtDNA Mutation
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