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Publikováno v:
INDIAN JOURNAL OF APPLIED RESEARCH. :18-20
Background : TBCK-related encephalopathy is a very rare condition recently diagnosed effecting the paediatric age group. It was rst discovered in 2015 by Saudi scientists who identied the role of TBCK gene mutation in a family of 13 members wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2fb1fd649e1182e647684223113a7a9
https://doi.org/10.36106/ijar/7300702
https://doi.org/10.36106/ijar/7300702
