https://vorinostatinhibitor.co....m/pituitary-hyperpla
qPCR analysis validated the absence of a copy number in this specific region, while his elder brother and parents exhibited normal copy numbers. This child's SSR4-CDG condition is strongly suspected to stem from the deletion of the SSR4 gene fragment located in the Xq28 region. It is highly plausible that the deletion of the fragment encompassing the SSR4 gene within the Xq28 chromosomal region played a crucial role in causin