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Figure 2 | Lipids in Health and Disease

Figure 2

From: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Figure 2

Pedigree of the Chinese family with retinitis pigmentosa associated with mutations in the C5L2 gene. Genotypes are shown beneath the symbols. Affected individuals are represented by black symbols, unaffected ones by unfilled; squares signify males, circles females. Arrows mark the index patients. M refers to the mutant allele, and + means normal allele.

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Lipids in Health and Disease

ISSN: 1476-511X