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Accession: PRJNA177196 ID: 177196

NHLBI GO-ESP: Family Studies (Atypical Cystic Fibrosis) (human)

See Genome Information for Homo sapiens
Cystic fibrosis (CF) patients without detectable disease-causing mutations in CFTR present a clinical phenotype very similar to, but possibly discrete from, classic CF. More...
AccessionPRJNA177196; dbGaP: phs000556
Data TypePhenotype or Genotype
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionJOHNS HOPKINS UNIVERSITY
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments6
Other datasets
BioSample6
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases55
Data volume, Mbytes21026

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