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Severe hypertriglyceridaemia in a Greek infant: a clinical,biochemical and genetic study |
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| Authors: | Emmanuel?Kavazarakis mailto:emka@ath.forthnet.gr" title=" emka@ath.forthnet.gr" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,Stella?Stabouli,Dimitrios?Gourgiotis,Katerina?Roumeliotou,Joanne?Traeger-Synodinos,Apostolos?Bossios,Andrew?Fretzayas,Emmanuel?Kanavakis |
| Affiliation: | (1) 2nd Department of Paediatrics, Athens University Medical School, !["ldquo"]("/content/43env311lcjypnp7/xlarge8220.gif") P. and A. Kyriakou!["rdquo"]("/content/43env311lcjypnp7/xlarge8221.gif") Children!["rsquo"]("/content/43env311lcjypnp7/xlarge8217.gif") s Hospital, Thibon and Levadias, Goudi, 115 27 Athens , Greece |
| Abstract: | |
| Keywords: | Compound heterozygosity Familial chylomicronaemia Hypertriglyceridaemia Lipoprotein lipase Mutation |
| 本文献已被 PubMed SpringerLink 等数据库收录！ | |