M. A. Khan

Identification of two novel variants in GNPTAB underlying mucolipidosis II in a Pakistani family

N. Karim, M. Naeem, H. Cheema, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family

J. Al-Aama, M. Naeem, J. Ahmed, 2013, Diagnostic Pathology.

Genetic Testing of a Large Consanguineous Pakistani Family Affected with Mucolipidosis III Gamma Through Next-Generation Sequencing.

M. Naeem, A. Hussain, M. A. Khan, 2018, Genetic testing and molecular biomarkers.

Whole exome sequencing identified two novel homozygous missense variants in the same codon of CLCN7 underlying autosomal recessive infantile malignant osteopetrosis in a Pakistani family

M. Naeem, M. A. Khan, Aman Ullah, 2018, Molecular Biology Reports.

Whole exome sequencing identified two novel homozygous missense variants in the same codon of CLCN7 underlying autosomal recessive infantile malignant osteopetrosis in a Pakistani family

M. A. Khan, Muhammad Naeem, Aman Ullah, 2018, Molecular Biology Reports.

Microplasma-assisted synthesis of CuO nanostructures for catalytic degradation of organic dyes under solar irradiation

M. Naeem, T. Iqbal, M. Shafique, 2020, Journal of Solid State Electrochemistry.