Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Victoria H Williams"'
Autor:
William Zhu, Xiaoping Huang, Esther Yoon, Sara Bandres-Ciga, Cornelis Blauwendraat, Kimberly J Billingsley, Joshua H Cade, Beverly P Wu, Victoria H Williams, Alice B Schindler, Janet Brooks, J Raphael Gibbs, Dena G Hernandez, Debra Ehrlich, Andrew B Singleton, Derek P Narendra
Publikováno v:
Brain
PRKN mutations are the most common recessive cause of Parkinson’s disease and are a promising target for gene and cell replacement therapies. Identification of biallelic PRKN patients at the population scale, however, remains a challenge, as roughl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f628ca7e72e3405b2283a238596ac9eb
https://doi.org/10.1093/brain/awab456
https://doi.org/10.1093/brain/awab456
Autor:
Sara Bandres-Ciga, Alice B. Schindler, William Zhu, Andrew B. Singleton, Joshua H. Cade, Debra Ehrlich, Derek P. Narendra, Beverly P Wu, Cornelis Blauwendraat, Xiaoping Huang, J. Raphael Gibbs, Esther Yoon, Dena G. Hernandez, Janet Brooks, Victoria H. Williams
PRKN mutations are the most common recessive cause of Parkinson’s disease (PD) and are a promising target for gene and cell replacement therapies. Identification of biallelic PRKN patients (PRKN-PD) at the population scale, however, remains a chall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4ea4345efbaadeeb18091aee0e5aa65
https://doi.org/10.1101/2021.08.11.21261928
https://doi.org/10.1101/2021.08.11.21261928
