Acceso abierto

A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia


Cite

M Despotović
University of Rijeka, Faculty of MedicineRijeka, Croatia
N Pereza
Department of Medical Biology and Genetics, University of Rijeka, Faculty of MedicineRijeka, Croatia
B Peterlin
Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
S Ostojić
Department of Medical Biology and Genetics, University of Rijeka, Faculty of MedicineRijeka, Croatia
B Golob
Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
A Maver
Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
J Roganović
Department of Pediatrics, Clinical Hospital Center RijekaRijeka, Croatia
eISSN:
1311-0160
Idioma:
Inglés
Calendario de la edición:
2 veces al año
Temas de la revista:
Medicine, Basic Medical Science, other