Query author contributions in Reactome

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Details on Person Talim, Beril

Class:Id	Person:5615627
_displayName	Talim, Beril
_timestamp	2014-07-25 13:32:32
created	[InstanceEdit:5615549] Jassal, Bijay, 2014-07-25
firstname	Beril
initial	B
surname	Talim
(author)	[LiteratureReference:5615545] Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan [LiteratureReference:5617063] Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease [LiteratureReference:6785665] Brain involvement in muscular dystrophies with defective dystroglycan glycosylation [LiteratureReference:9940658] An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene
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No pathways have been reviewed or authored by Talim, Beril (5615627)