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RTN4IP1 deficiency causes a severe CI assembly defect

ABSTRACT: Here we used complexome profiling to characterize the functional consequences of RTN4IP1 mutations in RTN4IP1 cells.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Ilka Wittig

LAB HEAD: Robert Taylor

PROVIDER: PXD064861 | Pride | 2025-08-08

REPOSITORIES: Pride

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Dataset's files

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			Action	DRS
	Data_Analysis.xlsx	Xlsx
	Gel.jpg	Other
	MQ_txt_Output_Files.zip	Other
	P21_129_Newcastle_Sample1_01.raw	Raw
	P21_129_Newcastle_Sample1_02.raw	Raw

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