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Human Molecular Genetics|June 17, 1999
A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2U R Monani, C L Lorson, D W Parsons, et al.
Human Molecular Genetics|November 25, 2000
The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 bindingP J Young, N T Man, C L Lorson, et al.
Nature Genetics|May 20, 1998
SMN oligomerization defect correlates with spinal muscular atrophy severityC L Lorson, J Strasswimmer, J M Yao, et al.
Human Molecular Genetics|August 1, 1997
The survival motor neuron protein in spinal muscular atrophyD D Coovert, T T Le, P E McAndrew, et al.
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