Query author contributions in Reactome

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Details on Person Salih, Mustafa A

Class:Id	Person:4839781
_displayName	Salih, Mustafa A
_timestamp	2013-11-04 09:53:24
created	[InstanceEdit:4839807] Jassal, B, 2013-11-04
firstname	Mustafa A
initial	MA
surname	Salih
(author)	[LiteratureReference:4839814] Congenital disorder of glycosylation IIa: the trouble with diagnosing a dysmorphic inborn error of metabolism [LiteratureReference:5633222] Congenital myasthenic syndromes due to mutations in ALG2 and ALG14 [LiteratureReference:5688576] The clinical spectrum of homozygous HOXA1 mutations [LiteratureReference:8931643] Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan [LiteratureReference:8931663] POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations [LiteratureReference:8931688] Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
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No pathways have been reviewed or authored by Salih, Mustafa A (4839781)