SAMN04529995
External Id
dbGaP
INSDC center name
2016-03-03T00:25:54.380Z
INSDC first public
2023-08-28T11:47:33.870Z
INSDC last update
SRS1358445
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS1358445
SRA accession
DNA
analyte type
NINDS Hereditary Spastic Paraplegia
biospecimen repository
S36
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
1901959
gap_sample_id
1527672
gap_subject_id
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Case Set
study design
Spastic Paraplegia, Hereditary
study disease
Genome Studies in Hereditary Spastic Paraplegia
study name
Yes
subject is affected
S36
submitted sample id
I36
submitted subject id
NINDS Hereditary Spastic Paraplegia
submitter handle
DNA sample from Blood of a human female participant in the dbGaP study "Genome Studies in Hereditary Spastic Paraplegia"
title