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Accession: PRJEB34790 ID: 636318

Predictors for OWOB in children with Prader Willi Syndrome

Prader-Willi Syndrome (PWS) is a rare and complex neurodevelopmental genetic disorder and the most common syndromic form of obesity. More...
AccessionPRJEB34790
ScopeMonoisolate
SubmissionRegistration date: 1-Jun-2020
HKU
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments57
Other datasets
BioSample57
SRA Data Details
ParameterValue
Data volume, Gbases1
Data volume, Mbytes584

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