Query author contributions in Reactome

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Details on Person Brockington, Martin

Class:Id	Person:5615546
_displayName	Brockington, Martin
_timestamp	2014-07-25 13:31:29
created	[InstanceEdit:5615549] Jassal, Bijay, 2014-07-25
firstname	Martin
initial	M
surname	Brockington
(author)	[LiteratureReference:5615545] Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan [LiteratureReference:6785669] Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan [LiteratureReference:9940719] Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy [LiteratureReference:9940807] Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant
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No pathways have been reviewed or authored by Brockington, Martin (5615546)