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You searched for: Author/Creator Ly, Carolyn

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2. Characterizing the molecular phenotype of an Atp7aT985I conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX). Issue 9 (13th June 2016)

3. Charcot–Marie–tooth disease causing mutation (p.R158H) in pyruvate dehydrogenase kinase 3 (PDK3) affects synaptic transmission, ATP production and causes neurodegeneration in a CMTX6 C. elegans model. Issue 1 (13th August 2021)

4. Improved inherited peripheral neuropathy genetic diagnosis by whole‐exome sequencing. Issue 2 (14th January 2015)

5. Improved inherited peripheral neuropathy genetic diagnosis by whole‐exome sequencing. Issue 2 (14th January 2015)