SAMN01057738
External Id
dbGaP
INSDC center name
2012-06-26T06:23:00.173Z
INSDC first public
2024-05-04T07:14:16.847Z
INSDC last update
SRS348502
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS348502
SRA accession
DNA
analyte type
NINDS_DevBrainDisorders
biospecimen repository
4923
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
746843
gap_sample_id
610759
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
4923
submitted sample id
WDex004
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