未登录Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies
Vaseghi, Parisa; Habibi, Laleh; Neidich, Julie A.; Cao, Yang; Fattahi, Neda; Rashidi-Nezhad, Ramin; Salehnezhad, Tayebeh; Dalili, Hossein; Sharbaf, Fatemeh Rahimi; Zarkesh, Mohammad Reza; Malekian, Mahtash; Mokhberdezfuli, Mahdieh; Mehrtash, Amirhosein; Ardeshirdavani, Amin; Kariminejad, Roxana; Ghorbansabagh, Vafa; Sadeghimoghadam, Parvane; Naddaf, Amir; Shirvany, Tahereh Esmaeilnia; Mosayebi, Ziba; Sahebdel, Behrokh; Golshahi, Fatemeh; Shirazi, Mahboobeh; Shamel, Shirin; Moeini, Roksana; Heidari, Abolfazl; Daneshmand, Mohammad Ali; Ghasemi, Reza; Akrami, Seyed Mohammad; Rashidi-Nezhad, Ali
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收藏Is Amyloid-β an Innocent Bystander and Marker in Alzheimer's Disease? Is the Liability of Multivalent Cation Homeostasis and its Influence on Amyloid-β Function the Real Mechanism?
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