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

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1. A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression. Issue 5 (3rd May 2016)

4. Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities. (14th August 2018)

5. Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities. (14th August 2018)

8. Transcription–translation coupling: direct interactions of RNA polymerase with ribosomes and ribosomal subunits. Issue 19 (16th August 2017)