https://www.selleckchem.com/pr....oducts/mito-tempo.ht
We report on retinal disease progression in homozygous patients, providing valuable allele-specific insights. The least involved retinal disease is seen in patients homozygous for c.5714 + 5GA variant, a so-called "mild" variant which is sufficient to precipitate a STGD1 phenotype in the absence of other pathogenic variants in the coding region and intron/exon boundaries of ABCA4. The most severe retinal disease is observed in cases with ABCA4 c.[5461-10TC;5603AT] complex allele. We discuss the advantages of determining g
إعجاب
علق
شارك
