Harvard Catalyst Profiles

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A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites.

A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites. Eur J Hum Genet. 2011 Oct; 19(10):1045-51.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.