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Turkish Journal of Pediatrics, ISSN 0041-4301, 2017, Volume 59, Issue 3, pp. 338 - 341
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 05/2019, Volume 29, Issue 5, pp. 376 - 380
2 mutations cause the most frequent congenital muscular dystrophy subtype MDC1A and a variety of milder phenotypes, characterized by total or partial... 
LAMA2 | WES | Congenital muscular dystrophy type 1A | Laminin-α2 | POPULATION | NERVE | CONGENITAL MUSCULAR-DYSTROPHY | MEROSIN | NEUROSCIENCES | CLINICAL NEUROLOGY | Laminin-alpha 2 | NEUROPATHY | COHORT | SPECTRUM
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2003, Volume 13, Issue 3, pp. 207 - 215
Deficiency of laminin α2 is the cause of one of the most severe muscular dystrophies in humans and other species. It is not yet clear how particular mutations... 
Mice | Muscular dystrophy | Laminin α2 chain gene
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 10/2001, Volume 38, Issue 10, pp. 649 - 657
Initial reports of patients with laminin α2 chain (merosin) deficiency had a relatively homogeneous phenotype, with classical congenital muscular dystrophy... 
Merosin | Laminin α2 chain | Congenital muscular dystrophy | Skeletal muscle | Review
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1828, pp. 553 - 564
Phosphorodiamidate morpholino oligomer (PMO)-mediated exon skipping is among the more promising approaches available for the treatment of several neuromuscular... 
mouse | dy | Exon skipping | Eteplirsen | NS-065/NCNP-01 | Dystrophin | Laminin-α2 chain | Merosin-deficient congenital muscular dystrophy type 1A (MDC1A) | Phosphorodiamidate morpholino oligomer (PMO) | Index Medicus
Journal Article
FEBS Letters, ISSN 0014-5793, 1997, Volume 415, Issue 1, pp. 33 - 39
Using the gene targeting technique, we have generated a new mouse model of congenital muscular dystrophy (CMD), a null mutant for the laminin α2 chain. These... 
Laminin α2 chain | Basal lamina | Gene targeting | Skeletal muscle | Muscular dystrophy | Apoptosis
Journal Article
Frontiers in Neurology, ISSN 1664-2295, 2019, Volume 10, Issue MAY, pp. 470 - 470
Journal Article
Brain Research, ISSN 0006-8993, 04/2005, Volume 1042, Issue 1, pp. 23 - 28
Laminin α2-deficient congenital muscular dystrophy is a debilitating disease affecting both muscle and neural tissue as a result of mutations in the LAMA2... 
Congenital muscular dystrophy | Laminin α2 | Synaptic plasticity
Journal Article
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2006, Volume 342, Issue 2, pp. 489 - 502
Fukuyama-type congenital muscular dystrophy (FCMD) and laminin-α2 deficient congenital muscular dystrophy (MDC1A) are congenital muscular dystrophies (CMDs)... 
Fukuyama-type congenital muscular dystrophy | DNA microarray | Laminin-α2 deficient congenital muscular dystrophy
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2014, Volume 24, Issue 5, pp. 419 - 424
Journal Article
Brain and Development, ISSN 0387-7604, 2007, Volume 29, Issue 6, pp. 357 - 364
Congenital muscular dystrophy (CMD) due to merosin (laminin 2 chain) deficiency is an autosomal recessively inherited disorder characterized by severe muscular... 
Laminin α2 chain | Congenital muscular dystrophy | Leukoencephalopathy | MR spectroscopy
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 1997, Volume 7, Issue 3, pp. 169 - 175
Approximately half the cases of classical congenital muscular dystrophy (CMD) have a pronounced deficiency or absence of the laminin α2 chain of laminin-2... 
Merosin | Laminin | Congenital muscular dystrophy | Laminin α2
Journal Article