Platelet dysfunction, familial (with AML)

RUNX1 - familial platelet dysfunction with predisposition for AML

This test is available for the following conditions:

• Conditions > Hematological, hereditary > Platelet dysfunction, familial (with AML)
• Conditions > Oncogenetics > Platelet dysfunction, familial (with AML)

This product is also part of the following panels:

• WES hemostatic/thrombotic disorders (100.0% *)
• WES hereditary cancer (100.0% *)
• WES inherited bone marrow failure and/or predisposition to hematological malignancies (100.0% *)
• WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

• Sequence analysis of all coding exons and flanking intron-exon boundaries
• Deletion/duplication analysis (MLPA)

OMIM: 151385
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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