Research paperLate onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency
References (16)
- et al.
Expression of laminin subunits in congenital muscular dystrophy
Neuromuscular Disord.
(1995) - et al.
Diagnosis of merosin (laminin alpha-2) deficient congenital muscular dystrophy by skin biopsy
Lancet
(1996) Muscle disorders of childhood
(1995)- et al.
Congenital muscular dystrophy with merosin deficiency
C R Acad Sci Paris Life Sci
(1994) - et al.
Localisation of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
Hum. Mol. Genet.
(1994) - et al.
Readjusting the localisation of merosin (laminin α2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2
C R Acad Sci Paris Life Sci
(1995) - et al.
Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo
J. Cell Sci.
(1995)
There are more references available in the full text version of this article.
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