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1 Ergebnisse
1
APOA5 Q97X Mutation Identified through homozygosity mapping..:
Dussaillant Catalina
;
Serrano Valentina
;
Maiz Alberto
...
http://www.biomedcentral.com/1471-2350/13/106. , 2012
Link:
https://doi.org/10.1186/1471-2350-13-106
RT Journal T1
APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:76ce413d7fd44f2cbed87d34371288b8&Exemplar=1&LAN=DE A1 Dussaillant Catalina A1 Serrano Valentina A1 Maiz Alberto A1 Eyheramendy Susana A1 Cataldo Luis A1 Chavez Matías A1 Smalley Susan V A1 Fuentes Marcela A1 Rigotti Attilio A1 Rubio Lorena A1 Lagos Carlos F A1 Martinez José A1 Santos José PB BMC YR 2012 K1 Hypertriglyceridemia K1 Genetic K1 Chylomicronemia K1 Mutation K1 Homozygosity mapping K1 APOA5 K1 Internal medicine K1 RC31-1245 K1 Genetics K1 QH426-470 JF http://www.biomedcentral.com/1471-2350/13/106 LK http://dx.doi.org/https://doi.org/10.1186/1471-2350-13-106 DO https://doi.org/10.1186/1471-2350-13-106 SF ELIB - SuUB Bremen
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