Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sara Milojevic"'
Autor:
Sara Milojevic, Arijit Ghosh, Vedrana Makevic, Maja Stojkovic, Maria Capovilla, Tomislav Tosti, Dejan Budimirovic, Dragana Protic
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 14, p 7949 (2024)
Fragile X syndrome (FXS) is caused by the full mutation in the FMR1 gene on the Xq27.3 chromosome region. It is the most common monogenic cause of autism spectrum disorder (ASD) and inherited intellectual disability (ID). Besides ASD and ID and other
Externí odkaz:
https://doaj.org/article/ef7162aa2fa44d239b1b9c523b45fa57
Autor:
Maja Stojkovic, Milan Petrovic, Maria Capovilla, Sara Milojevic, Vedrana Makevic, Dejan B. Budimirovic, Louise Corscadden, Shuhan He, Dragana Protic
Publikováno v:
Biology, Vol 13, Iss 6, p 432 (2024)
Fragile X syndrome (FXS), the most common monogenic cause of inherited intellectual disability and autism spectrum disorder, is caused by a full mutation (>200 CGG repeats) in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene. Individuals with
Externí odkaz:
https://doaj.org/article/1af7cf936b0f46f084fd0eb8e156dd9c
Autor:
Jelena Trajković, Vedrana Makevic, Milica Pesic, Sofija Pavković-Lučić, Sara Milojevic, Smiljana Cvjetkovic, Randi Hagerman, Dejan B. Budimirovic, Dragana Protic
Publikováno v:
Genes, Vol 14, Iss 1, p 87 (2022)
Fragile X syndrome (FXS) is a global neurodevelopmental disorder caused by the expansion of CGG trinucleotide repeats (≥200) in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene. FXS is the hallmark of Fragile X-associated disorders (FXD) and
Externí odkaz:
https://doaj.org/article/0b503870fd834c73b08e190f28c19fb6