Cognitive Functions in Ataxia with Oculomotor Apraxia Type 2

Background: Ataxia with oculomotor apraxia type 2 (AOA2) is characterized by cerebellar atrophy, peripheral neuropathy, oculomotor apraxia, and elevated serum alpha-fetoprotein (AFP) levels. The disease is caused by a recessive mutation in the senataxin gene. Since it is a very rare cerebellar disor...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Klivényi, Peter, Nemeth, Dezso, Sefcsik, Tamas, Janacsek, Karolina, Hoffmann, Ildiko, Haden, Gabor Peter, Londe, Zsuzsa, Vecsei, Laszlo
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Frontiers Research Foundation 2012
विषय:
Neuroscience
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3449493/
https://ncbi.nlm.nih.gov/pubmed/23015802
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2012.00125
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