A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report by Osama Y. Muthaffar, Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Abrar Ashi, Abrar Ashi, Muhammad Imran Naseer, Muhammad Imran Naseer

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Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families by Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Qaiser Zaman, Qaiser Zaman, Qaiser Zaman, Hamza Khan, Sabar Khan, Gauhar Rehman, Nabeel Tariq, Mashal Ahmad, Muhammad Owais, Najumuddin, Osama Yousef Muthaffar, Fehmida Bibi, Fehmida Bibi, Rin Khang, Seung Woo Ryu, Muhammad Imran Naseer, Muhammad Imran Naseer, Musharraf Jelani

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Combinatorial Therapeutic Potential of Stem Cells and Benzimidazol Derivatives for the Reduction of Liver Fibrosis by Maryam Iqbal, Sulaiman Shams, Huma Rafiq, Momin Khan, Shahid Khan, Umer Sadique Khattak, Sahib Gul Afridi, Fehmida Bibi, Angham Abdulrhman Abdulkareem, Muhammad Imran Naseer

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Phenotypic Classification of Eye Colour and Developmental Validation of the Irisplex System on Population Living in Malakand Division, Pakistan by Murad Ali Rahat, Fazal Akbar, Akhtar Rasool, Muhammad Ilyas, Allah Rakha, Sulaiman Shams, Musharraf Jelani, Fehmida Bibi, Bader H. Shirah, Angham Abdulrhman Abdulkareem, Muhammad Imran Naseer, Muhammad Israr

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