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Accession: PRJEB1956 ID: 284452

Exome sequencing in congenital hyperinsulinism

Congenital hyperinsulinism of infancy (CHI) is a rare disorder characterized by severe hypoglycemia due to inappropriate insulin secretion. More...

Accession	PRJEB1956
Data Type	Exome
Scope	Monoisolate
Submission	Registration date: 20-May-2015 Institute for Biomedical Technologies at the Italian CNR Consiglio Nazionale delle Ricerche, Italy

Project Data:

Parameter	Value
Data volume, Gbases	44
Data volume, Mbytes	16236

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