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Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology
2014
270 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
14.97
Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology | Researchclopedia
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The University of Melbourne
Elizabeth Fitzpatrick
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Murdoch Children's Research Institute
Stefan A. Haas
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Max Planck Institute for Molecular Genetics
Kate Pope
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Murdoch Children's Research Institute
Kirk J. Hogan
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University of Wisconsin–Madison
Ronald G. Gregg
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University of Louisville
Catherine Bromhead
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Walter and Eliza Hall Institute of Medical Research
David S. Wargowski
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University of Wisconsin–Madison
Christopher Lawrence
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Royal Hobart Hospital
Paul A. James
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The Royal Melbourne Hospital
Andrew Churchyard
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Monash Children’s Hospital
Yujing Gao
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Murdoch Children's Research Institute
Dean Phelan
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The University of Melbourne
Greta Gillies
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Murdoch Children's Research Institute
Nicholas Salce
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Murdoch Children's Research Institute
Lynn Stanford
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Oregon Health & Science University
Ashley P.L. Marsh
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The University of Melbourne
Maria Lidia Mignogna
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Roche (Switzerland)
Susan J. Hayflick
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Oregon Health & Science University
Richard J. Leventer
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Royal Children's Hospital
Martin B. Delatycki
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The University of Melbourne
George D. Mellick
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Griffith University
Vera M. Kalscheuer
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Max Planck Institute for Molecular Genetics
Patrizia D’Adamo
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Dulbecco Telethon Institute
Melanie Bahlo
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The University of Melbourne
David J. Amor
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The University of Melbourne
Paul J. Lockhart
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The University of Melbourne