Fingerprint
Dive into the research topics of 'Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases
Firoz Kabir, Inayat Ullah, Shahbaz Ali, Alexander D.H. Gottsch, Muhammad Asif Naeem, Muhammad Zaman Assir, Shaheen N. Khan, Javed Akram, Sheikh Riazuddin, Radha Ayyagari, J. Fielding Hejtmancik, S. Amer Riazuddin
Research output: Contribution to journal › Article › peer-review
11
Scopus
citations