2017 International Congress

June 4-8, 2017. Vancouver, BC.

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Tuesday, June 6, 2017

1:45pm-3:15pm: Whole Exome Sequencing (WES) identifies a TUBB4A Mutation in two Saudi siblings with hypomyelinating leukodystrophy associated with atrophy of basal ganglia and cerebellum.

Z. Aldaajani, E.-S. Ali (Dhahran, Saudi Arabia)

Genetics (Non-PD) · Exhibit Hall C

1:45pm-3:15pm: Whole exome sequencing in essential tremor.

I. Alfradique-Dunham, L. Robak, A. Kaw, O. Fagbongbe, Z. Coban Akdemir, E. Young, J. Lupski, J. Jankovic, J. Shulman (Houston, TX, USA)

Genetics (Non-PD) · Exhibit Hall C

1:45pm-3:15pm: WILSON’S DISEASE: A Mongolian case

U. Dashdorj, S. Jambal (Ulaanbaatar 51, Mongolia)

Rare Genetic and Metabolic Diseases · Exhibit Hall C

1:45pm-3:15pm: Сase of myotonic dystrophy

A. Jusupova (Bishkek, Kyrgyzstan)

Genetics (Non-PD) · Exhibit Hall C