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Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy.

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Raker,  V. A.
Department of Cellular Biochemistry, MPI for biophysical chemistry, Max Planck Society;

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Luehrmann,  R.
Department of Cellular Biochemistry, MPI for biophysical chemistry, Max Planck Society;

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Citation

Buehler, D., Raker, V. A., Luehrmann, R., & Fischer, U. (1999). Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy. Human Molecular Genetics, 8, 2351-2357.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0012-FA4C-C
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