TY  - RPRT
TI  - Exome sequencing identifies a homozygous splice site variant in RP1 as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani family.
AU  - Abdur Rashid
AU  - Asad Munir
AU  - Muhammad Zahid
AU  - Mukhtar Ullah
AU  - Atta Ur Rehman
PY  - 2025
DO  - 10.1080/07853890.2025.2470953
UR  - https://pubmed.ncbi.nlm.nih.gov/40029043/
ID  - 40029043
ER  -