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Accession: PRJNA171811 ID: 171811

Homo sapiens (human)

A mutation in the c-Fos gene associated with congenital generalized lipodystrophy

See Genome Information for Homo sapiens
Lipodystrophies resemble syndromes of disturbed adipocyte biology or development and severe congenital forms (CGL) lack adipose tissue. More...
AccessionPRJNA171811; GEO: GSE39825
Data TypeTranscriptome or Gene expression
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsKnebel B et al., "A mutation in the c-fos gene associated with congenital generalized lipodystrophy.", Orphanet J Rare Dis, 2013 Aug 7;8:119
SubmissionRegistration date: 2-Aug-2012
Cinical Biochemistry and Pathobiochemistry, German Diabetes Center
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots126250
Data volume, Processed Mbytes2
Data volume, Supplementary Mbytes33

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