New GATA1 mutation in codon 2 leads to the earliest known premature stop codon in transient myeloproliferative disorder.

Hoeller, Sylvia

New GATA1 mutation in codon 2 leads to the earliest known premature stop codon in transient myeloproliferative disorder. [electronic resource] - Blood Oct 2009 - 3717-8 p. digital

Publication Type: Case Reports; Comment; Letter

1528-0020

10.1182/blood-2009-07-233833 doi


Codon, Nonsense--genetics
Fatal Outcome
GATA1 Transcription Factor--genetics
Humans
Infant, Newborn
Male
Mutation--genetics
Myeloproliferative Disorders--complications