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J.JACL.2017.08.008
J.JACL.2017.08.008
http://dx.doi.org/10.1016/J.JACL.2017.08.008
A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia.
P356
Q49891108-8F3D4AE1-E989-4B5F-9007-18BB46B10CB3
P356
J.JACL.2017.08.008
http://dx.doi.org/10.1016/J.JACL.2017.08.008