A significant neurodevelopmental disorder associated with a South Asian founder mutation in the UFMylation adaptor CDK5RAP3 - Poll - MDSpire

A significant neurodevelopmental disorder associated with a South Asian founder mutation in the UFMylation adaptor CDK5RAP3

  • By

  • Michaela Yuen

  • Katharine Zhang

  • Rhett G. Marchant

  • Ryosuke Ishimura

  • Mark Graham

  • May Aung-Htut

  • Samantha Bryen

  • Rocio Rius

  • Lee Marshall

  • Nader Aryamanesh

  • Gregory Dziaduch

  • Himanshu Joshi

  • Ben Weisburd

  • Steve D. Wilton

  • Meredith Wilson

  • Russell Gear

  • Lucy Hennington

  • Stephanie Lau

  • Helen Doyle

  • Michael Krivanek

  • Richard J. Leventer

  • Susan M. White

  • Sarah A. Sandaradura

  • Masaaki Komatsu

  • Frances J. Evesson

  • Sandra T. Cooper

  • April 27, 2026

  • 0 min

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Original Source(s)

A significant neurodevelopmental disorder associated with a South Asian founder mutation in the UFMylation adaptor CDK5RAP3

  • by Michaela Yuen, Katharine Zhang, Rhett G. Marchant, Ryosuke Ishimura, Mark Graham, May Aung-Htut, Samantha Bryen, Rocio Rius, Lee Marshall, Nader Aryamanesh, Gregory Dziaduch, Himanshu Joshi, Ben Weisburd, Steve D. Wilton, Meredith Wilson, Russell Gear, Lucy Hennington, Stephanie Lau, Helen Doyle, Michael Krivanek, Richard J. Leventer, Susan M. White, Sarah A. Sandaradura, Masaaki Komatsu, Frances J. Evesson, Sandra T. Cooper

  • April 27, 2026

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