PRR14L mutations are associated with chromosome 22... (ID 516624) - BioProject

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Accession: PRJEB30453 ID: 516624

PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age related clonal hematopoiesis and myeloid neoplasia

Whole exome sequencing of 5 MDS/MPN patients to identify the target of chromosome 22 acquired uniparental disomy (22aUPD). More...

Accession	PRJEB30453
Scope	Monoisolate
Submission	Registration date: 23-Jan-2019 University of Southampton

Project Data:

Parameter	Value
Data volume, Gbases	61
Data volume, Mbytes	64422

Supplemental Content

PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, ...
PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age related clonal hematopoiesis and myeloid neoplasia
PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age related clonal hematopoiesis and myeloid neoplasia

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