Association of Pro12Ala polymorphism in peroxisome proliferator activated receptor gamma with proliferative diabetic retinopathy

por Tariq, Khadija, Malik, Saira Bano, Ali, Syeda Hafiza Benish, Maqsood, Sundas Ejaz, Azam, Aisha, Muslim, Irfan, Khan, Muhammad Shakil, Azam, Maleeha, Waheed, Nadia Khalida, Qamar, Raheel
Publicado 2013

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa

por Azam, Maleeha, Khan, Muhammad Imran, Gal, Andreas, Hussain, Alamdar, Shah, Syed Tahir Abbas, Khan, Muhammad Shakil, Sadeque, Ahmed, Bokhari, Habib, Collin, Rob W.J., Orth, Ulrike, van Genderen, Maria M., den Hollander, A.I., Cremers, Frans P. M., Qamar, Raheel
Publicado 2009