Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B.


YILMAZ B., Mungan N., Di L., MAGNOLO L., ARTUSO L., BERNARDIS I., ...Daha Fazla

Clinica chimica acta; international journal of clinical chemistry, cilt.452, ss.185-90, 2016 (SCI-Expanded) identifier identifier identifier