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Accession: PRJNA1013221 ID: 1013221

To EXPLORING MITONUCLEAR GENETIC FACTORS IN LEBER'S HEREDITARY OPTIC NEUROPATHY: INSIGHTS FROM COMPREHENSIVE PROFILING OF UNIQUE CASES

This study investigate the genetic basis of thirty distinct LHON cases through comprehensive sequencing to identify mito-nuclear genetic factors involved in the disease pathogenesis. More...
AccessionPRJNA1013221
Data TypeRaw sequence reads
ScopeMultispecies
SubmissionRegistration date: 6-Sep-2023
Aravind medical research foundation
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments10
Other datasets
BioSample10
SRA Data Details
ParameterValue
Data volume, Gbases103
Data volume, Mbytes39634

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