Faletra, F., Snider, K., Shyng, S., Bruno, I., Athanasakis, E., Gasparini, P., . . . Burlina, A. (2012). Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations.
استشهاد بنمط شيكاغوFaletra, Flavio, et al. Co-inheritance of Two ABCC8 Mutations Causing an Unresponsive Congenital Hyperinsulinism: Clinical and Functional Characterization of Two Novel ABCC8 Mutations. 2012.
MLA استشهادFaletra, Flavio, et al. Co-inheritance of Two ABCC8 Mutations Causing an Unresponsive Congenital Hyperinsulinism: Clinical and Functional Characterization of Two Novel ABCC8 Mutations. 2012.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.