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In vivo selection reveals combinatorial controls that define a critical exon in the spinal muscular atrophy genes

Humans have two near identical copies of the survival of motor neuron (SMN) gene, SMN1 and SMN2. In spinal muscular atrophy (SMA), SMN2 is not able to compensate for the loss of SMN1 due to an inhibitory mutation at position 6 (C6U mutation in transcript) of exon 7. We have recently shown that C6U c...

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Bibliografiset tiedot
Päätekijät: SINGH, NATALIA N., ANDROPHY, ELLIOT J., SINGH, RAVINDRA N.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Copyright 2004 by RNA Society 2004
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Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1370618/
https://ncbi.nlm.nih.gov/pubmed/15272122
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.7580704
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