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Paper Details

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
Science
390
2014
HSP, HSP genes, HSPs, Hereditary spastic paraplegias, candidate genes, corticospinal motor neuron disease, neurodegenerative disorders, neurodegenerative motor neuron diseases, nucleotide, putative HSP genes
Animals, Axons, Biological Transport, Cohort Studies, Exome, Gene Regulatory Networks, Genetic Association Studies, Humans, Motor Neuron Disease, Mutation, Neurons, Nucleotides, Pyramidal Tracts, Sequence Analysis, DNA, Spastic Paraplegia, Hereditary, Synapses, Transcriptome, Zebrafish
Author NameAffiliation
Gaia NovarinoHoward Hughes Medical Institute, University of California
Ali G FenstermakerHoward Hughes Medical Institute, University of California
Maha S ZakiClinical Genetics Department, National Research Center
Matan HofreeUniversity of California
Matan HofreeUniversity of California
Jennifer L SilhavyHoward Hughes Medical Institute, University of California
Lucila Ohno-MachadoHoward Hughes Medical Institute, University of California
Mostafa AbdellateefHoward Hughes Medical Institute, University of California
Basak RostiHoward Hughes Medical Institute, University of California
Eric ScottHoward Hughes Medical Institute, University of California
Lobna MansourCairo University Children's Hospital
Amira MasriUniversity of Jordan
H??lya KayseriliIstanbul University
Jumana Y Al-AamaKing Abdulaziz University
Ghada M H Abdel-SalamClinical Genetics Department, National Research Center
Ariana Kariminejad
Majdi KaraTripoli Children's Hospital
B??lent KaraKocaeli University
Bita Bozorgmehri
Tawfeg Ben-OmranClinical and Metabolic Genetics Division, Hamad Medical Corporation
Faezeh Mojahedi
Iman G MahmoudCairo University Children's Hospital
Naima BouslamUniversite Mohammed V Souissi
Ahmed BouhoucheUniversite Mohammed V Souissi
Ali BenomarUniversite Mohammed V Souissi
Sylvain HaneinCentre de Recherche de l'Institut du Cerveau et de la Moelle epiniere, INSERM U1127, CNRS UMR7225 UPMC Univ Paris VI UMR_S975
Laure RaymondCentre de Recherche de l'Institut du Cerveau et de la Moelle epiniere, INSERM U1127, CNRS UMR7225 UPMC Univ Paris VI UMR_S975
Sylvie ForlaniCentre de Recherche de l'Institut du Cerveau et de la Moelle epiniere, INSERM U1127, CNRS UMR7225 UPMC Univ Paris VI UMR_S975
Massimo MascaroHoward Hughes Medical Institute, University of California
Laila SelimCairo University Children's Hospital
Nabila ShehataSaudi German Hospital
Nasir A S Al-AllawiUniversity of Dohuk
Parayil Sankaran BinduNational Institute of Mental Health and Neurosciences
Matloob AzamWah Medical College
Murat GunelYale University School of Medicine
Ahmet Okay CaglayanYale University School of Medicine
Kaya BilguvarYale University School of Medicine
Asl??han TolunBogazici University
Mahmoud Y IssaClinical Genetics Department, National Research Center
Jana SchrothHoward Hughes Medical Institute, University of California
Emily G SpencerHoward Hughes Medical Institute, University of California
Rasim O RostiHoward Hughes Medical Institute, University of California
Naiara AkizuHoward Hughes Medical Institute, University of California
Keith K VauxHoward Hughes Medical Institute, University of California
Anide JohansenHoward Hughes Medical Institute, University of California
Alice A KohHoward Hughes Medical Institute, University of California
Hisham MegahedClinical Genetics Department, National Research Center
Alexandra DurrCentre de Recherche de l'Institut du Cerveau et de la Moelle epiniere, INSERM U1127, CNRS UMR7225 UPMC Univ Paris VI UMR_S975
Alexandra DurrAssistance Publique-Hopitaux de Paris, Pitie-Salpetriere Hospital
Alexis BriceCentre de Recherche de l'Institut du Cerveau et de la Moelle epiniere, INSERM U1127, CNRS UMR7225 UPMC Univ Paris VI UMR_S975
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