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α‐tropomyosin gene (TPM3) mutation in an infant with nemaline myopathy by Sulaiman Almobarak, Jonathan Hu, Kristopher D. Langdon, Lee‐Cyn Ang, Craig Campbell
Published 2021-03-01
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MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients by Carl O. Olson, Shervin Pejhan, Daniel Kroft, Kimia Sheikholeslami, Kimia Sheikholeslami, David Fuss, Marjorie Buist, Annan Ali Sher, Marc R. Del Bigio, Yehezkel Sztainberg, Victoria Mok Siu, Lee Cyn Ang, Marianne Sabourin-Felix, Tom Moss, Mojgan Rastegar
Published 2018-12-01
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