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Genetic factors underlying premature MI in Greek families without vessel disease

The study will analyse by exome sequencing 8 Greek family members with an excess of potentially damaging mutations relating to premature MI and no vessel disease, to identify genetic factors underlying this condition. This is a follow on from project GPMI-NVD

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Wellcome Trust Sanger Institute Data Sharing Policy

Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS00001000478 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00000483042 cram 2.0 GB
EGAF00000483043 cram 1.8 GB
EGAF00000483044 cram 2.0 GB
EGAF00000483045 cram 2.1 GB
EGAF00000483046 cram 2.0 GB
EGAF00000483047 cram 1.9 GB
EGAF00000483048 cram 2.0 GB
EGAF00000483049 cram 2.0 GB
EGAF00000487111 cram 2.1 GB
EGAF00000487112 cram 1.8 GB
EGAF00000487113 cram 2.0 GB
EGAF00000487114 cram 2.2 GB
EGAF00000487115 cram 2.1 GB
EGAF00000487116 cram 1.9 GB
EGAF00000487117 cram 2.1 GB
EGAF00000487118 cram 2.1 GB
16 Files (32.2 GB)