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Fragile X syndrome is the most common form of inherited mental retardation in men. The molecular mechanism underlying the disease is an amplification of a polymorphic trinucleotide repeat (CGG)n located at 5' end of FMR1 which promotes transcriptiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238f795456f48aa0e24f913b856dd997
https://pubmed.ncbi.nlm.nih.gov/12119565
https://pubmed.ncbi.nlm.nih.gov/12119565
