SAMN37155283
External Id
dbGaP
INSDC center name
2023-08-25T20:42:15.763Z
INSDC first public
2023-10-19T21:38:16.537Z
INSDC last update
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
ERS17004658
SRA accession
DNA
analyte type
NINDS Hereditary Spastic Paraplegia
biospecimen repository
2022030419277
biospecimen repository sample id
Blood
body site
phs001080
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
5662340
gap_sample_id
4632129
gap_subject_id
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
sex
Case Set
study design
Spastic Paraplegia, Hereditary
study disease
Genome Studies in Hereditary Spastic Paraplegia
study name
Yes
subject is affected
2022030419277
submitted sample id
2022030419277
submitted subject id
NINDS Hereditary Spastic Paraplegia
submitter handle
DNA sample from Blood of a human male participant in the dbGaP study "Genome Studies in Hereditary Spastic Paraplegia"
title