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Table 2 Mean telomere length of control and immortalized cell lines.

From: Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders

Name

Clone

Number of divisions

Telomere length, kb, mean ± SEM

CTRL

C25Cl48

127

17.6 ± 0.3

CMD

CMDCl12

42

20.8 ± 1.7

DMD

DMDCl2

57.9

10.3 ± 0.1

FSHD

FSHDCl17

37.9

24.8 ± 1.6

LGMD2B

LGMD2Cl11

27.4

17.2 ± 3.0

OPMD

OPMDCl2

47.6

20.0 ± 0.5

  1. CMD, congenital muscular dystrophy; DMD, Duchenne muscular dystrophy; FSHD, fascioscapulohumeral muscular dystrophy; LGMD2B, limb-girdle muscular dystrophy type 2B; OPMD, oculopharyngeal muscular dystrophy