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. 2009 Apr 20;8(7):1708–1718. doi: 10.1074/mcp.M900122-MCP200

Table I. Summary of patient samples.

Clinical data are provided where available. M, male; F, female, n/a, not applicable.

Identifier Diagnosis Age of onset Age of death Post-mortem interval Gender
years years h
HSB 120 Adenoleukodystrophy 56 M
CABM-BR19 Adult NCL 20 33 F
CABM-BR8 Adult NCL Late 30s 50s M
HSB 2356 Adult NCL 33 40 8 M
HSB 4165 Adult NCL 29 53 6.5 M
UMB 338 Alexander disease 6.2 12 M
UMB 613 Alexander disease 14 7 M
UMB 575 Krabbe disease 1.4 4 M
CABM-BR21 Late infantile NCL (CLN2) M
UMB 784 Late infantile NCL (CLN2) 5.3 4 F
UMB 563 Mucopolysaccharidosis IIIA 11.3 12 F
UMB 821 Neuromuscular disorder, undiagnosed 3.6 8 F
HSB 238 Normal control n/a 43 F
HSB 298 Normal control n/a 19 M
HSB 304 Normal control n/a 22 M
HSB 331 Normal control n/a 16 M
HSB 712 Normal control n/a 16 M
HSB 863 Normal control n/a 40 M
UMB 1270 Seizure disorder 22 22 F
UMB 506 Sudanophilic leukodystrophy 0.4 5 F
HSB 148 Tay-Sachs disease 0.6 1.9 F
HSB 1183 Unknown epilepsy 0.2 1 F
CABM-BR1 Unknown NCL M
CABM-BR11 Unknown NCL F
CABM-BR23 Unknown NCL
CABM-BR24 Unknown NCL 24 20.6 F
CABM-BR25 Unknown NCL 8 16.5 F
CABM-BR32 Unknown NCL F
CABM-BR33 Unknown NCL 12.4 F
CABM-BR34 Unknown NCL 7.5 M
CABM-BR36 Unknown NCL F
HSB 4391 Unknown NCL 12 F
HSB 2548 Variant late infantile NCL 7 25 F