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Whole‐exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome
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Download from www.researchgate.netDépistage néonatal en France : quel avenir ?
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Download from www.researchgate.netPhenotype and genotype in 101 males with X-linked creatine transporter deficiency
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Download from www.ncbi.nlm.nih.govTNF-α- and tumor-induced skeletal muscle atrophy involves sphingolipid metabolism.
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