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Your search keyword '"Perlman, Seth J"' showing total 5 results

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5 results on '"Perlman, Seth J"'

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1. Targeted long-read sequencing identifies missing disease-causing variation

2. Clinical RNA sequencing clarifies variants of uncertain significance identified by prior testing

3. Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis

4. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

5. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

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