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Alterations in White Matter Microstructure in Neurofibromatosis-1

Neurofibromatosis (NF1) represents the most common single gene cause of learning disabilities. NF1 patients have impairments in frontal lobe based cognitive functions such as attention, working memory, and inhibition. Due to its well–characterized genetic etiology, investigations of NF1 may shed lig...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Karlsgodt, Katherine H., Rosser, Tena, Lutkenhoff, Evan S., Cannon, Tyrone D., Silva, Alcino, Bearden, Carrie E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3477133/
https://ncbi.nlm.nih.gov/pubmed/23094098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0047854
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