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Hyperventilation-athetosis in ASXL3 deficiency (Bainbridge-Ropers) syndrome

Rubina Dad1, Susan Walker1, Stephen W Scherer1

  • 1Atta-ur Rahman School of Applied Biosciences (R.D., M.J.H.), National University of Sciences and Technology (NUST), Islamabad, Pakistan; Program in Genetics and Genome Biology (R.D.) and The Centre for Applied Genomics, Genetics and Genome Biology (S.W., S.W.S.), The Hospital for Sick Children, Department of Molecular Genetics (S.W.S.), and McLaughlin Centre (S.W.S.), University of Toronto, Ontario, Canada; Department of Neurolgy (S.Y.K.), Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Gyeonggi-do, Republic of Korea; Program in Genetics and Genome Biology (B.A.M.), Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Ontario, Canada; and Departments of Pediatrics, Neurology, and Neurotherapeutics (B.A.M.), University of Texas Southwestern, Dallas.

Neurology. Genetics
|September 29, 2017
PubMed
Abstract

No abstract available in PubMed .

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