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Letter to the Editor

Reply to Brown et al: ‘Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis’

ORCID Icon, , , , , , , , , , , , , , & show all
Pages 248-249 | Received 05 Oct 2019, Accepted 06 Oct 2019, Published online: 23 Oct 2019

References

  • Bellissimo DC, Speck NA. RUNX1 mutations in inherited and sporadic leukemia. Front Cell Dev Biol. 2017;5:111.
  • Garcia JS, Madzo J, Cooper D, et al. Pre-donor evaluation of an HLA matched sibling identifies a novel inherited RUNX1 mutation encoding a missense mutation found outside of the RUNT domain in familial platelet disorder. Blood. 2010; 116:2709 [ASH Annual Meeting Abstracts].

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