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Accession: PRJNA160053 ID: 160053

Genetics of Human Developmental Brain Disorders (human)

See Genome Information for Homo sapiens
Developmental brain malformations are at the core of significant neurological diseases affecting many families in the United States and around the world. It is known that epilepsy, specific learning deficits and intellectual disability, cerebral palsy, and abnormalities of brain volume can be attributed in many cases to pathological malformations of the cerebral cortex. Although these consequences, such as epilepsy and intellectual disability, might appear broadly in the population as due to complex traits, this study's focus on those associated with cortical malformations highlights individual developmental pathways likely represented by innumerable and rare Mendelian alleles. Research has thus far uncovered dozens of genes responsible for these conditions and dissected the mechanisms underlying early cortical development in animals. More...
AccessionPRJNA160053; dbGaP: phs000492
TypeUmbrella project (Subtype:Authorized Access)
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 16-Dec-2012
NHGRI
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments87
Other datasets
BioSample87
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases680
Data volume, Tbytes0.32
Genetics of Human Developmental Brain Disorders encompasses the following sub-project:
Project TypeNumber of Projects
Phenotype or Genotype1
BioProject
accession
OrganismTitle
PRJNA160055Homo sapiensGenetics of Human Developmental Brain Disorders (HARVARD MEDICAL SCHOOL)

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