Molecular analysis of SMA patients without homozygous SMN1 deletions using a new strategy for identification of SMN1 subtle mutations
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P. Bénit | A. Munnich | O. Clermont | P. Burlet | P. Saugier-Veber | V. Cusin | Dominique Chanterau
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P. Bénit | A. Munnich | O. Clermont | P. Burlet | P. Saugier-Veber | V. Cusin | Dominique Chanterau