Mutations in CWC27 result in spectrum of conditions
Articles / Genetics / Retinitis pigmentosa

Mutations in CWC27 result in spectrum of conditions

Mingchu Xu searches for genes linked to retinitis pigmentosa, a condition of the retina characterized by progressive development of night blindness and tunnel vision, sometimes from the early age of 2. Retinitis pigmentosa is the most common inherited disorder of the retina; it affects nearly 1 in 4,000 people, and more than 1 million are visually … Continue reading

Improving the view on the genetic causes of retinitis pigmentosa
Articles / Genetics / Retinitis pigmentosa

Improving the view on the genetic causes of retinitis pigmentosa

Progressive development of night blindness and tunnel vision, sometimes from the early age of 2, are trademarks of retinitis pigmentosa. Being the most common inherited disorder of the retina, retinitis pigmentosa affects nearly 1 in 4,000 people. More than 1 million are visually impaired around the world due to this untreatable disease. A number of … Continue reading