Neurology / Neuropediatrics
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L-2-hydroxyglutaric aciduria (sequence analysis of L2HGDH gene)
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Lacticacidemia due to PDX1 deficiency (sequence analysis of PDHX gene)
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Late-onset alzheimer disease susceptibility (sequence analysis of NOS3 gene)
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Legius syndrome (deletion/duplication analysis of SPRED1 gene)
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Legius syndrome (sequence analysis of SPRED1 gene)
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Leigh syndrome (m.8993T>G and m.8993T>C mutation on MT-ATP6 gene)
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Leigh syndrome (NGS panel for 11 genes)
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Leigh syndrome (sequence analysis of COX15 gene)
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Leigh syndrome (sequence analysis of FOXRED1 gene)
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Leigh syndrome (sequence analysis of MTND3 gene)
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Leigh syndrome (sequence analysis of NDUFA10 gene)
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Leigh syndrome (sequence analysis of NDUFA13 gene)
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Leigh syndrome (sequence analysis of NDUFA2 gene)
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Leigh syndrome (sequence analysis of NDUFA9 gene)
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Leigh syndrome (sequence analysis of NDUFAF1 gene)
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Leigh syndrome (sequence analysis of NDUFAF2 gene)
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Leigh syndrome (sequence analysis of NDUFAF3 gene)
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Leigh syndrome (sequence analysis of NDUFAF6 gene)
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Leigh syndrome (sequence analysis of NDUFS3 gene)
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Leigh syndrome (sequence analysis of NDUFS4 gene)
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