Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Behzad Ezzatian"'
Publikováno v:
Basic and Clinical Neuroscience, Vol 13, Iss 2, Pp 269-274 (2022)
Introduction: Alexander disease is a heterogeneous group of diseases with various manifestations based on the age of disease onset. This rare leukodystrophy syndrome with mutations in the GFAP gene could present with developmental delay and seizure i
Externí odkaz:
https://doaj.org/article/2bbd8a2697f44c83bf54a13d2656c296
Publikováno v:
Basic and Clinical Neuroscience Journal. 13:269-274
Introduction: Alexander disease is a heterogeneous group of diseases with various manifestations based on the age of disease onset. This rare leukodystrophy syndrome with mutations in the GFAP gene could present with developmental delay and seizure i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::602ddd66a16519e8dea75b632c716890
https://doi.org/10.32598/bcn.2021.1551.1
https://doi.org/10.32598/bcn.2021.1551.1