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Whole-exome sequencing identifies Max mutations as a cause of hereditary pheochromocytoma

Identifiers: SRA: ERP000569
BioProject: PRJEB2461
SPANISH NATIONAL CENTER FOR BIOTECHNOLOGY - CSIC: E-MTAB-591
Study Type: 
Other
Submission: ERA023806
Description: Whole exome sequencing identification of Max mutations and further validation in pheochromocytoma patients
Center Project: Whole-exome sequencing identifies Max mutations as a cause of hereditary pheochromocytoma
External Link: E-MTAB-591 in ArrayExpress

Related SRA data

Experiments:
20
Runs:
20 (92.8Gbp; 63.8Gb)