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. 2016 Feb 3;12(2):e1005416. doi: 10.1371/journal.ppat.1005416

Table 2. Clinical and molecular features of heterozygous (MV) iCJD cases analyzed.

Case ID Number Gender Age at Onset a Duration b Molecular Sub-classification Brain Region c PrPSc Type d M129 (%) e
15 M 33 8 iCJD MV2 CC 2d 39 ± 9
16 F 30 12 iCJD MV2 CC 2d 38 ± 14
17 M 32 16 iCJD MV2 CC 2+1 46 ± 3
18 M 28 16 iCJD MV2 CC 2d 36 ± 5
19 F 27 32 iCJD MV2 CC 2d 66 ± 4
20 F 32 23 iCJD MV2 CC 2+1 39 ± 6

aAge of onset in years.

bDisease duration in months.

cCC = cerebral cortex.

dPrPSc typing according to the method of Parchi et al. [33].

eMean percentage ± SD of PrPSc with M129.

There was no significant correlation of percentage PrPSc-M129 with iCJD type, age of onset, or disease duration (p>0.3).