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The University of Chicago

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

One or more keywords matched the following properties of A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites.

Property	Value
has major subject area list	Founder Effect; Genetic Carrier Screening; Haplotypes; Muscular Atrophy, Spinal; Sequence Deletion; Survival of Motor Neuron 1 Protein

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Survival of Motor Neuron 1 Protein