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Expanding the genotype-phenotype landscape of PDE10A- associated movement disorders

Author:Bohlega, Saeed   Al- Qahtani, Zainah   Guzmán-Vega, Francisco J.   Ramakrishnan, Reshmi   Abusrair, Ali   Aldosari, Haya   AlDakheel, Amaal   Al-Qahtani, Salma   Monies, Dorota   Arold, Stefan   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.004  

Author Institution:King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia  King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia  University of Calgary, Calgary, AB, Canada  

Identification of novel compound heterozygous mutation in Niemann-Pick disease type C gene

Author:Abusrair, Ali   Amorelli, Gabriel   Sarna, Justyna   

Session Name:P14: Movement Disorders: Miscellaneous Movement Disorders 2  

Topic:Movement Disorders  

Program Number:P14.006  

Author Institution:University of Calgary, Calgary, AB, Canada