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Fig. 1 | Lipids in Health and Disease

Fig. 1

From: Clinical, biochemical and molecular analysis of two infants with familial chylomicronemia syndrome

Fig. 1

Partical nucleotide sequence of LPL gene in the probands. a KD-4 (proband A) was found compound heterozygosity of p.Arg270His and p.Trp421* mutations on LPL gene. Left: Chromatogram of DNA sequence analysis of LPL gene mutations. Arrow indicates the mutation site. KD-4 and KD-1 (father of proband A) were heterozygous for c.809G > A, KD-2 (mother of proband A) and KD-3 (brother of proband A) were normal.Right: KD-2, KD-3, KD-4 were heterozygous for c.1262G > A and KD-1 was normal. b Chromatogram of DNA sequence analysis of LPL gene mutations. Arrow indicates the mutation site. KD-7 (proband B) and KD-6 (father of proband B) were heterozygous for c.836T > G, KD-5 (mother of proband B) as normal

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