Young S.C. ea, 1990
Young S.C., Hubl S.T., Smith R.S. et. al. Familial hypodetalipoproteinemia caused by mutation in the apolipoprotein B gene that result in a truncated species of apolipoprotein B (B31) : A unique mutation that helps to define the portion of apolipoprotein B molecule required for the formation of buoyant, triglycerid-rich lipoproteins // J. Clin. Invest. 1990. V.85. P.933-942.
Смотрите также:
