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. 2018 Oct 30;9:1533. doi: 10.3389/fphys.2018.01533

Table 1.

Striated and cardiac muscle laminopathies caused by mutations in nuclear envelope proteins.

LMNA Mutations
AD-Emery Dreifuss Muscular Dystrophy (AD-EDMD) Bonne et al., 1999
AR-Emery Dreifuss Muscular Dystrophy (AR-EDMD) Raffaele Di Barletta et al., 2000
Limb-girdle muscular dystrophy type 1B (LGMD1B) van der Kooi et al., 1997; Muchir et al., 2000
LMNA-associated congenital muscular dystrophy (L-CMD) Quijano-Roy et al., 2008
Dilated-cardiomyopathy (DCM-CD) Fatkin et al., 1999
EMD Mutations
X-linked Emery-Dreifuss Muscular Dystrophy (XL-EDMD) Bione et al., 1994
X-linked Limb-girdle muscular dystrophy (X-LGMD) Ura et al., 2007
LAP2 Mutations
LAP-2α: Dilated cardiomyopathy (DCM) Taylor et al., 2005
SYNE Mutations
Nesprin 1α and 2β: Emery-Dreifuss Muscular Dystrophy-like Zhang et al., 2007
Nesprin 1α: Dilated cardiomyopathy Puckelwartz et al., 2010
TMEM43 Mutations
Emery-Dreifuss Muscular Dystrophy-like Liang et al., 2011
FHL1 Mutations
Emery-Dreifuss Muscular Dystrophy Gueneau et al., 2009