CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder-Reference-Cited by-同舟云学术

CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder

Published:2015-02 Issue:2 Volume:96 Page:245-257
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

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.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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