A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia.
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A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年學術文章
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name
A novel homozygous mutation ca ...... me gestational hyperlipidemia.
@en
A novel homozygous mutation ca ...... me gestational hyperlipidemia.
@nl
type
label
A novel homozygous mutation ca ...... me gestational hyperlipidemia.
@en
A novel homozygous mutation ca ...... me gestational hyperlipidemia.
@nl
prefLabel
A novel homozygous mutation ca ...... me gestational hyperlipidemia.
@en
A novel homozygous mutation ca ...... me gestational hyperlipidemia.
@nl
P2093
P1476
A novel homozygous mutation ca ...... me gestational hyperlipidemia.
@en
P2093
David Rial-Crestelo
Francisco Blanco-Vaca
Ildefonso Santos-Recuero
P304
1475-1479.e3
P356
10.1016/J.JACL.2017.08.008
P407
P577
2017-08-24T00:00:00Z