SAMN04530002
External Id
dbGaP
INSDC center name
2016-03-03T00:25:55.110Z
INSDC first public
2023-08-28T11:47:36.170Z
INSDC last update
SRS1358397
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS1358397
SRA accession
DNA
analyte type
NINDS Hereditary Spastic Paraplegia
biospecimen repository
S84
biospecimen repository sample id
Blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs001080
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
1902012
gap_sample_id
1527725
gap_subject_id
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
sex
Case Set
study design
Spastic Paraplegia, Hereditary
study disease
Genome Studies in Hereditary Spastic Paraplegia
study name
Yes
subject is affected
S84
submitted sample id
I84
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