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American Journal of Human Genetics|March 21, 2000
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42M Brockington, C A Sewry, R Herrmann, et al.
Brain : a Journal of Neurology|January 1, 1997
Hereditary demyelinating neuropathy of infancy. A genetically complex syndromeJ Tyson, D Ellis, U Fairbrother, et al.
Lancet (London, England)|March 2, 1996
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsyC A Sewry, J Philpot, L M Sorokin, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular-eye-brain loci: report of three siblingsV Ruggieri, F Lubieniecki, F Meli, et al.
Neuromuscular Disorders : NMD|July 21, 2009
Muscle MRI in FHL1-linked reducing body myopathyG Astrea, J Schessl, E Clement, et al.
Brain : a Journal of Neurology|January 22, 2009
Reduced expression of fukutin related protein in mice results in a model for fukutin related protein associated muscular dystrophiesM R Ackroyd, L Skordis, M Kaluarachchi, et al.
Neuropediatrics|August 1, 1997
Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophyC A Sewry, M D'Alessandro, L A Wilson, et al.
American Journal of Human Genetics|June 19, 1998
Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36B Moghadaszadeh, I Desguerre, H Topaloglu, et al.
Human Immunology|June 1, 1993
Combinations of specific DRB1, DQA1, DQB1 haplotypes are associated with insulin-dependent diabetes mellitus in SardiniaF Cucca, F Muntoni, R Lampis, et al.
Biochemical and Biophysical Research Communications|November 4, 2000
Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophyG Lattanzi, F Muntoni, P Sabatelli, et al.
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