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You searched for: Author/Creator Hou, Ya‐Ming

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1. A Mitochondrial tRNA Mutation Causes Axonal CMT in a Large Venezuelan Family. Issue 4 (29th August 2020)

2. A Recurrent Loss‐of‐Function Alanyl‐tRNA Synthetase (AARS) Mutation in Patients with Charcot‐Marie‐Tooth Disease Type 2N (CMT2N). Issue 4 (18th February 2014)

3. Compound heterozygosity for loss‐of‐function GARS variants results in a multisystem developmental syndrome that includes severe growth retardation. Issue 10 (14th July 2017)

4. Cover Image, Volume 38, Issue 10. Issue 10 (14th September 2017)