Search

Search Constraints

You searched for: Author/Creator Rupar, C. Anthony

Search Results

3. Exome sequencing identifies NFS1 deficiency in a novel Fe‐S cluster disease, infantile mitochondrial complex II/III deficiency. Issue 1 (18th November 2013)

4. Health Care for Mitochondrial Disorders in Canada: A Survey of Physicians. (November 2019)

6. Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia. Issue 9 (24th July 2014)