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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 8, 2024. (Total: 232338Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Fragile X Syndrome and BDNF[original query]
The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome.
Epilepsy research 2009 Jul 85 (1): 114-7.
Louhivuori Verna, Arvio Maria, Soronen Pia, Oksanen Virpi, Paunio Tiina, Castrén Maija
Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role?
Epilepsy & behavior : E&B 2011 Nov 22 (3): 581-3.
Tondo Mireia, Poo Pilar, Naudó Montserrat, Ferrando Teresa, Genovés Jordi, Molero Marta, Martorell Lore
Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome.
Brain & development 2017 Feb .
AlOlaby Reem Rafik, Sweha Stefan R, Silva Marisol, Durbin-Johnson Blythe, Yrigollen Carolyn M, Pretto Dalyir, Hagerman Randi J, Tassone Flo
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