AAAAAA

   
Results: 1-2 |
Results: 2
A SINGLE G-NUCLEOTIDE TO A-NUCLEOTIDE TRANSITION IN EXON IV OF THE LECITHIN - CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE RESULTS IN AN ARG(140) TO HIS SUBSTITUTION AND CAUSES LCAT-DEFICIENCY
Authors: STEYRER E HAUBENWALLNER S HORL G GIESSAUF W KOSTNER GM ZECHNER R
Citation: E. Steyrer et al., A SINGLE G-NUCLEOTIDE TO A-NUCLEOTIDE TRANSITION IN EXON IV OF THE LECITHIN - CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE RESULTS IN AN ARG(140) TO HIS SUBSTITUTION AND CAUSES LCAT-DEFICIENCY, Human genetics, 96(1), 1995, pp. 105-109
A NOVEL MISSENSE MUTATION IN THE GENE FOR LIPOPROTEIN-LIPASE RESULTING IN A HIGHLY CONSERVATIVE AMINO-ACID SUBSTITUTION (ASP(180) -] GLU) CAUSES FAMILIAL CHYLOMICRONEMIA (TYPE-I HYPERLIPOPROTEINEMIA)
Authors: HAUBENWALLNER S HORL G SHACHTER NS PRESTA E FRIED SK HOFLER G KOSTNER GM BRESLOW JL ZECHNER R
Citation: S. Haubenwallner et al., A NOVEL MISSENSE MUTATION IN THE GENE FOR LIPOPROTEIN-LIPASE RESULTING IN A HIGHLY CONSERVATIVE AMINO-ACID SUBSTITUTION (ASP(180) -] GLU) CAUSES FAMILIAL CHYLOMICRONEMIA (TYPE-I HYPERLIPOPROTEINEMIA), Genomics, 18(2), 1993, pp. 392-396
Risultati: 1-2 |