Query author contributions in Reactome

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Details on Person Houlden, Henry

Class:Id	Person:3165245
_displayName	Houlden, Henry
_timestamp	2013-02-22 16:13:37
created	[InstanceEdit:3165246] Jassal, B, 2013-02-22
firstname	Henry
initial	H
surname	Houlden
(author)	[LiteratureReference:3165248] Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54 [LiteratureReference:5626445] Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11 [LiteratureReference:6803186] NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease [LiteratureReference:9949735] NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease
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No pathways have been reviewed or authored by Houlden, Henry (3165245)