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Carnitine palmitoyltransferase II deficiency in a prenatal case with polycystic kidney disease‐like phenotype
Author(s) -
He Yi,
Li DongZhi
Publication year - 2020
Publication title -
congenital anomalies
Language(s) - English
Resource type - Journals
eISSN - 1741-4520
pISSN - 0914-3505
DOI - 10.1111/cga.12357
Subject(s) - china , medicine , pediatrics , family medicine , political science , law
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