Query author contributions in Reactome

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Details on Person Raidt, Johanna

Class:Id	Person:9945658
_displayName	Raidt, Johanna
_timestamp	2025-04-16 19:18:13
created	[InstanceEdit:9945652] Rothfels, Karen, 2025-04-16
firstname	Johanna
initial	J
surname	Raidt
(author)	[LiteratureReference:9945663] MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia [LiteratureReference:9966692] CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module [LiteratureReference:9966698] CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module [LiteratureReference:9968814] DYX1C1 is required for axonemal dynein assembly and ciliary motility [LiteratureReference:9969018] ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6 [LiteratureReference:9969740] Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms
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No pathways have been reviewed or authored by Raidt, Johanna (9945658)