Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ashwin R. Sharma"'
Autor:
Maham Rais, Jonathan W. Lovelace, Xinghao S. Shuai, Walker Woodard, Steven Bishay, Leo Estrada, Ashwin R. Sharma, Austin Nguy, Anna Kulinich, Patricia S. Pirbhoy, Arnold R. Palacios, David L. Nelson, Khaleel A. Razak, Iryna M. Ethell
Publikováno v:
Neurobiology of Disease, Vol 162, Iss , Pp 105577- (2022)
Background: Fragile X syndrome (FXS) is a leading genetic cause of autism and intellectual disability with cortical hyperexcitability and sensory hypersensitivity attributed to loss and hypofunction of inhibitory parvalbumin-expressing (PV) cells. Ou
Externí odkaz:
https://doaj.org/article/59d4773c4e2a47b0bd3f51d0b57d3dd3
Autor:
Maham Rais, Jonathan W. Lovelace, Xinghao S. Shuai, Walker Woodard, Steven Bishay, Leo Estrada, Ashwin R. Sharma, Austin Nguy, Anna Kulinich, Patricia S. Pirbhoy, Arnold R. Palacios, David L. Nelson, Khaleel A. Razak, Iryna M. Ethell
Publikováno v:
Neurobiology of Disease, Vol 162, Iss, Pp 105577-(2022)
Background: Fragile X syndrome (FXS) is a leading genetic cause of autism and intellectual disability with cortical hyperexcitability and sensory hypersensitivity attributed to loss and hypofunction of inhibitory parvalbumin-expressing (PV) cells. Ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa3d2f2e791b992c246f6384bc95158b
https://pubmed.ncbi.nlm.nih.gov/34871737
https://pubmed.ncbi.nlm.nih.gov/34871737