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pro vyhledávání: '"Shinji Saitoh"'
Publikováno v:
eNeurologicalSci, Vol 22, Iss , Pp 100298- (2021)
Background: Angelman syndrome (AS) is neurodevelopmental disorder, causal gene of which is maternally expressed UBE3A. A majority of patients results from the large deletion of relevant chromosome which includes GABAA receptor subunit genes (GABARs)
Externí odkaz:
https://doaj.org/article/3a934c4521be410d8fb3dcde9ea2f280
Publikováno v:
eNeurologicalSci
eNeurologicalSci, Vol 22, Iss, Pp 100298-(2021)
eNeurologicalSci, Vol 22, Iss, Pp 100298-(2021)
Background Angelman syndrome (AS) is neurodevelopmental disorder, causal gene of which is maternally expressed UBE3A. A majority of patients results from the large deletion of relevant chromosome which includes GABAA receptor subunit genes (GABARs) a