Neurodegeneration associated with genetic defects in phospholipase A(2)

OBJECTIVE: Mutations in the gene encoding phospholipase A(2) group VI (PLA2G6) are associated with two childhood neurologic disorders: infantile neuroaxonal dystrophy (INAD) and idiopathic neurodegeneration with brain iron accumulation (NBIA). INAD is a severe progressive psychomotor disorder in whi...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Gregory, A, Westaway, S K., Holm, I E., Kotzbauer, P T., Hogarth, P, Sonek, S, Coryell, J C., Nguyen, T M., Nardocci, N, Zorzi, G, Rodriguez, D, Desguerre, I, Bertini, E, Simonati, A, Levinson, B, Dias, C, Barbot, C, Carrilho, I, Santos, M, Malik, I, Gitschier, J, Hayflick, S J.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Academy of Neurology 2008
विषय:
Articles
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC2676964/
https://ncbi.nlm.nih.gov/pubmed/18799783
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000327094.67726.28
टैग : टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!
लोड हो रहा है...

समान संसाधन