USH2A

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Study for People with USH2A Mutations

By Dr. Steve Rose on April 4, 2017 USH2A is a target for retinal-disease researchers, because mutations in the gene are the most common cause of Usher syndrome type 2, which causes combined vision loss from retinitis pigmentosa (RP) and hearing loss from inner ear dysfunction. Also, USH2A mutations are a leading cause of RP [...]

به وسیله |2017-07-12T08:49:04+04:30جولای 12th, 2017|English, دیگر مطالب سایت|بدون دیدگاه