APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.
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APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.
description
2012 nî lūn-bûn
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2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի նոյեմբերին հրատարակված գիտական հոդված
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2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@ast
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@en
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@nl
type
label
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@ast
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@en
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@nl
prefLabel
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@ast
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@en
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@nl
P2093
P2860
P50
P356
P1433
P1476
APOA5 Q97X mutation identified ...... Chilean consanguineous family.
@en
P2093
Alberto Maiz
Attilio Rigotti
Catalina Dussaillant
José Alfredo Martinez
Lorena Rubio
Marcela Fuentes
Matías Chavez
Susan V Smalley
Susana Eyheramendy
Valentina Serrano
P2860
P2888
P356
10.1186/1471-2350-13-106
P577
2012-11-15T00:00:00Z
P5875
P6179
1046914583