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                                       Details for article 3 of 15 found articles
 
 
  Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability
 
 
Title: Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability
Author: Law, Rosalind
Dixon-Salazar, Tracy
Jerber, Julie
Cai, Na
Abbasi, Ansar A.
Zaki, Maha S.
Mittal, Kirti
Gabriel, Stacey B.
Rafiq, Muhammad Arshad
Khan, Valeed
Nguyen, Maria
Ali, Ghazanfar
Copeland, Brett
Scott, Eric
Vasli, Nasim
Mikhailov, Anna
Khan, Muhammad Nasim
Andrade, Danielle M.
Ayaz, Muhammad
Ansar, Muhammad
Ayub, Muhammad
Vincent, John B.
Gleeson, Joseph G.
Appeared in: The American journal of human genetics
Paging: Volume 95 (2014) nr. 6 pages 8 p.
Year: 2014
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 3 of 15 found articles
 
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