Neurocognitive Function in Dopamine-β-Hydroxylase Deficiency

Dopamine-β-hydroxylase (DβH) deficiency is a rare genetic syndrome characterized by the complete absence of norepinephrine in the peripheral and the central nervous system. DβH-deficient patients suffer from several physical symptoms, which can be treated successfully with L-threo-3,4-dihydroxypheny...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Jepma, Marieke, Deinum, Jaap, Asplund, Christopher L, Rombouts, Serge ARB, Tamsma, Jouke T, Tjeerdema, Nathanja, Spapé, Michiel M, Garland, Emily M, Robertson, David, Lenders, Jacques WM, Nieuwenhuis, Sander
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2011
Aiheet:
Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3138665/
https://ncbi.nlm.nih.gov/pubmed/21471955
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/npp.2011.42
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