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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population

Figure 1

Pedigrees of Pakistani families carrying TYR mutations. Pedigrees of ten multi-generational families segregating recessive nonsyndromic OCA due to mutations in the TYR gene. Filled and empty symbols represent affected and unaffected individuals, respectively. Double lines indicate consanguineous marriages. Asterisks indicate subjects enrolled in the protocol that contributed DNA samples.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172