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Sewry Caroline A.
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Caroline A.
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http://hub.abes.fr/bmj/periodical/jnnp/2008/volume_79/issue_1/B35A82167AFA4C40E053120B220AF6DD/authorship/4
http://hub.abes.fr/bmj/periodical/jnnp/2004/volume_75/issue_12/B35A58F059B40DA1E053120B220AC3BE/authorship/3
http://hub.abes.fr/oup/periodical/brainj/2007/volume_130/issue_8/101093brainawm096/authorship/3
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_2/101093brainawn325/authorship/3
http://hub.abes.fr/oup/periodical/hmg/2006/volume_15/issue_18/101093hmgddl221/authorship/5
http://hub.abes.fr/oup/periodical/brainj/2007/volume_130/issue_10/101093brainawm212/authorship/17
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_25/101093hmg10252879/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_21/101093hmgddg307/authorship/11
http://hub.abes.fr/oup/periodical/brainj/2007/volume_130/issue_6/101093brainawm094/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_25/101093hmg10252851/authorship/18
http://hub.abes.fr/oup/periodical/hmg/2007/volume_16/issue_10/101093hmgddm092/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_4/101093hmgddg032/authorship/8
http://hub.abes.fr/springer/periodical/10735/1993/volume_25/issue_8/B8D3CDE5D11A196DE053120B220AD839/authorship/5
http://hub.abes.fr/springer/periodical/10735/1993/volume_25/issue_8/B8D3CDE5D11E196DE053120B220AD839/authorship/5
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Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Refining genotype-phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
Distal myopathy caused by homozygous missense mutations in the nebulin gene
Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor
Characterization of recessive RYR1 mutations in core myopathies
Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis
Characterization of recessive RYR1 mutations in core myopathies
Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle
Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle
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