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                                       Details for article 1 of 49 found articles
 
 
  ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies
 
 
Title: ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies
Author: Lemire, Gabrielle
Ito, Yoko A.
Marshall, Aren E.
Chrestian, Nicolas
Stanley, Valentina
Brady, Lauren
Tarnopolsky, Mark
Curry, Cynthia J.
Hartley, Taila
Mears, Wendy
Derksen, Alexa
Rioux, Nadie
Laflamme, Nataly
Hutchison, Harrol T.
Pais, Lynn S.
Zaki, Maha S.
Sultan, Tipu
Dane, Adrie D.
Gleeson, Joseph G.
Vaz, Frédéric M.
Kernohan, Kristin D.
Bernard, Geneviève
Boycott, Kym M.
Appeared in: The American journal of human genetics
Paging: Volume 108 () nr. 10 pages 2017-2023
Year: 2021
Contents:
Publisher: American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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