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Autor:
D S, Osypenko, A V, Dovgan, N I, Kononenko, A V, Dromaretsky, M, Matvieienko, O A, Rybachuk, J, Zhang, S M, Korogod, V, Venkataraman, P, Belan
Publikováno v:
Neurobiology of disease. 132
A recent report of autosomal-recessive primary isolated dystonia (DYT2 dystonia) identified mutations in HPCA, a gene encoding a neuronal calcium sensor protein, hippocalcin (HPCA), as the cause of this disease. However, how mutant HPCA leads to neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::202c14107f391ad56124750622b43a70
https://pubmed.ncbi.nlm.nih.gov/31301343
https://pubmed.ncbi.nlm.nih.gov/31301343
