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                                       Details for article 4 of 17 found articles
 
 
  CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
 
 
Title: CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
Author: Wortmann, Saskia B.
Ziętkiewicz, Szymon
Kousi, Maria
Szklarczyk, Radek
Haack, Tobias B.
Gersting, Søren W.
Muntau, Ania C.
Rakovic, Aleksandar
Renkema, G. Herma
Rodenburg, Richard J.
Strom, Tim M.
Meitinger, Thomas
Rubio-Gozalbo, M. Estela
Chrusciel, Elzbieta
Distelmaier, Felix
Golzio, Christelle
Jansen, Joop H.
van Karnebeek, Clara
Lillquist, Yolanda
Lücke, Thomas
Õunap, Katrin
Zordania, Riina
Yaplito-Lee, Joy
van Bokhoven, Hans
Spelbrink, Johannes N.
Vaz, Frédéric M.
Pras-Raves, Mia
Ploski, Rafal
Pronicka, Ewa
Klein, Christine
Willemsen, Michel A.A.P.
de Brouwer, Arjan P.M.
Prokisch, Holger
Katsanis, Nicholas
Wevers, Ron A.
Appeared in: The American journal of human genetics
Paging: Volume 96 (2015) nr. 2 pages 13 p.
Year: 2015
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 4 of 17 found articles
 
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