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. 2017 May 2;12(5):e0176526. doi: 10.1371/journal.pone.0176526

Fig 1. Frequency of CLN2 disease-associated mutations.

Fig 1

(A) Allele frequency of CLN2 disease mutations demonstrates a predominance of nonsense (29%) and missense (22%) mutations. (B) The most common CLN2 disease mutations consists of either the intronic transversion c.509-1G>C that results in altered transcript splicing or the exonic transition c.622C>T that results in the p.R208X nonsense mutation.