Query author contributions in Reactome

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Details on Person Smith, Richard J H

Class:Id	Person:2534361
_displayName	Smith, Richard J H
_timestamp	2012-10-25 15:24:04
created	[InstanceEdit:2534342] Gillespie, ME, 2012-10-25
firstname	Richard J H
initial	RJ
surname	Smith
(author)	[LiteratureReference:2534367] Genetic male infertility and mutation of CATSPER ion channels [LiteratureReference:4416504] A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration [LiteratureReference:5624263] Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice [LiteratureReference:8955013] A catechol-O-methyltransferase that is essential for auditory function in mice and humans [LiteratureReference:9662987] Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus [LiteratureReference:9663056] Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse
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No pathways have been reviewed or authored by Smith, Richard J H (2534361)