Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

Bibliographic Details
Main Authors: Farag, Heba Gamal, Froehler, Sebastian, Oexle, Konrad, Ravindran, Ethiraj, Schindler, Detlev, Staab, Timo, Huebner, Angela, Kraemer, Nadine, Chen, Wei, Kaindl, Angela M
Format: Online
Language:English
Published: BioMed Central 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225825/
id pubmed-4225825
recordtype oai_dc
spelling pubmed-42258252014-11-11 Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation Farag, Heba Gamal Froehler, Sebastian Oexle, Konrad Ravindran, Ethiraj Schindler, Detlev Staab, Timo Huebner, Angela Kraemer, Nadine Chen, Wei Kaindl, Angela M Research BioMed Central 2013-11-14 /pmc/articles/PMC4225825/ /pubmed/24228726 http://dx.doi.org/10.1186/1750-1172-8-178 Text en Copyright © 2013 Farag et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Farag, Heba Gamal
Froehler, Sebastian
Oexle, Konrad
Ravindran, Ethiraj
Schindler, Detlev
Staab, Timo
Huebner, Angela
Kraemer, Nadine
Chen, Wei
Kaindl, Angela M
spellingShingle Farag, Heba Gamal
Froehler, Sebastian
Oexle, Konrad
Ravindran, Ethiraj
Schindler, Detlev
Staab, Timo
Huebner, Angela
Kraemer, Nadine
Chen, Wei
Kaindl, Angela M
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
author_facet Farag, Heba Gamal
Froehler, Sebastian
Oexle, Konrad
Ravindran, Ethiraj
Schindler, Detlev
Staab, Timo
Huebner, Angela
Kraemer, Nadine
Chen, Wei
Kaindl, Angela M
author_sort Farag, Heba Gamal
title Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
title_short Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
title_full Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
title_fullStr Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
title_full_unstemmed Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
title_sort abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous wdr62 gene mutation
description
publisher BioMed Central
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225825/
_version_ 1613154339218522112

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