Query author contributions in Reactome

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Details on Person Gecz, Jozef

Class:Id	Person:4836525
_displayName	Gecz, Jozef
_timestamp	2013-10-30 11:57:59
created	[InstanceEdit:4836510] Jassal, B, 2013-10-30
firstname	Jozef
initial	J
surname	Gecz
(author)	[LiteratureReference:4836527] Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation [LiteratureReference:5661048] SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome [LiteratureReference:5696561] La FAM fatale: USP9X in development and disease [LiteratureReference:8870295] Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1 [LiteratureReference:8877777] Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly [LiteratureReference:8955442] CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling [LiteratureReference:8955690] COMMD1 is linked to the WASH complex and regulates endosomal trafficking of the copper transporter ATP7A [LiteratureReference:9022830] Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males [LiteratureReference:9988808] PHF6 mutations in T-cell acute lymphoblastic leukemia
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No pathways have been reviewed or authored by Gecz, Jozef (4836525)