Determination of SMN1 and SMN2 copy number using TaqMan™ technology
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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3. Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscle atrophy in the absence of SMN1;Cartegni;Nat Genet,2002
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5. Implementation of SMA carrier testing in genetic laboratories: comparison of two methods for quantifying the SMN1 gene;Cusco;Hum Mutat,2002
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