The molecular lesion is a C to G missense point mutation in exon 16 (2038C-G) of the gene leading to a predicted leucine to valine exchange (L680V). (J:82809, J:237905)
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The molecular lesion is a C to G missense point mutation in exon 16 (2038C-G) of the gene leading to a predicted leucine to valine exchange (L680V). (J:82809, J:237905)