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9522ff8172d6a8d8a6308ad92d8b575b National Human Genome Research Institute {"start": "2018-11-07T20:00:00", "end": "2018-11-07T21:00:00"}

Gahl, William A., M.D., Ph.D. Clinical Director

Dr. Gahl studies the natural history, diagnosis, and treatment of rare genetic disorders such as cystinosis, Hermansky-Pudlak Syndrome, sialic acid storage diseases, GNE myopathy, and disorders of platelets and pigmentation. He also investigates undiagnosed disorders under the aegis of the NIH Undiagnosed Diseases Program and Network, and pursues new disease discovery.

https://videocast.nih.gov/watch=28773 https://www.genome.gov/10005723/gahl--group/