Homo sapiens (ID 163353) - BioProject

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Accession: PRJNA163353 ID: 163353

Homo sapiens (human)

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Myotonic Dystrophy Type-2 (DM2) is an autosomal dominant disease caused by the expansion of a CCTG tetraplet repeat. More...

Accession	PRJNA163353; GEO: GSE37794
Data Type	Transcriptome or Gene expression
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications	Greco S et al., "Deregulated microRNAs in myotonic dystrophy type 2.", PLoS One, 2012;7(6):e39732
Submission	Registration date: 6-May-2012 Molecular Cardiology, IRCCS-Policlinico San Donato
Relevance	Medical

Project Data:

Parameter	Value
Data volume, Spots	6935
Data volume, Processed Mbytes	1
Data volume, Supplementary Mbytes	1

Supplemental Content

Homo sapiens
Homo sapiens
microRNAs expression profile in Myotonic Dystrophy type-2 (DM2) patients

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