Researchers Link Gene Mutation to Retinitis Pigmentosa in Southwestern U.S. Hispanic Families

 Researchers Link Gene Mutation to Retinitis Pigmentosa in Southwestern U.S. Hispanic Families

Researchers at The University of Texas Health Science Center at Houston (UTHealth) School of Public Health have reportedly found 36 percent of Hispanic families in the U.S. with a common form of retinitis pigmentosa got the disease because they carry a mutation of the arrestin-1 gene.

The research team reportedly studied a cohort of 300 families in the U.S. with retinitis pigmentosa, and found 3 percent exhibited a mutation of the arrestin-1 gene. However, they reportedly found more than 36 percent of Hispanic families from the cohort exhibited the arestin-1 mutation and they all came from areas in the Southwestern U.S., such as Texas, Arizona and Southern California.

The study was recently published in the journal Investigative Ophthalmology & Visual Science.

Click here to read the full press release.

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Source: The University of Texas Health Science Center at Houston (UTHealth)

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