BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes-Reference-Cited by-同舟云学术

BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes

Published:2021-03 Issue: Volume:99 Page:102.e1-102.e10
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Khani Marzieh,Shamshiri Hosein,Taheri Hanieh,Hardy John,Bras Jose Tomas,Carmona Susana,Moazzeni Hamidreza,Alavi Afagh,Heshmati Ali,Taghizadeh Peyman,Nilipour Yalda,Ghazanfari Tooba,Shahabi Majid,Okhovat Ali Asghar,Rohani Mohammad,Valle Giorgio,Boostani Reza,Abdi Siamak,Eshghi Shaghayegh,Nafissi Shahriar,Elahi Elahe

Funder

Iran National Science Foundation

Tehran University of Medical Sciences and Health Services

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

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