Reactome: A Curated Pathway Database
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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person Chung, Eddie M K

Class:IdPerson:9945646
_displayNameChung, Eddie M K
_timestamp2025-04-16 19:18:12
created[InstanceEdit:9945652] Rothfels, Karen, 2025-04-16
firstnameEddie M K
initialEM
surnameChung
(author)[LiteratureReference:9945663] MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia
[LiteratureReference:9968797] CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms
[LiteratureReference:9968905] Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia
[LiteratureReference:9968914] Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia
[LiteratureReference:9969764] X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3
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No pathways have been reviewed or authored by Chung, Eddie M K (9945646)