SAMN01057739
External Id
dbGaP
INSDC center name
2012-06-26T06:23:00.397Z
INSDC first public
2024-05-04T07:14:17.150Z
INSDC last update
SRS348504
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS348504
SRA accession
DNA
analyte type
NINDS_DevBrainDisorders
biospecimen repository
324
biospecimen repository sample id
Blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs000455
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
746840
gap_sample_id
610763
gap_subject_id
SNP Genotypes (NGS)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
sex
Prospective Longitudinal Cohort
study design
Lissencephaly
http://www.orpha.net/ORDO/Orphanet_102009
study disease
Molecular Genetic Studies of Developmental Brain Disorders
study name
Yes
subject is affected
324
submitted sample id
WDex024
submitted subject id
NINDS_DevBrainDisorders
submitter handle
DNA sample from Blood of a human male participant in the dbGaP study Molecular Genetic Studies of Developmental Brain Disorders
title