A. Latif

发表

Molecular analysis of lipoid proteinosis: identification of a novel nonsense mutation in the ECM1 gene in a Pakistani family

M. Naeem, M. Ajmal, A. Hameed, 2011, Diagnostic pathology.

In silico characterization of a novel pathogenic deletion mutation identified in XPA gene in a Pakistani family with severe xeroderma pigmentosum

S. Malik, N. Ahmad, A. Hameed, 2013, Journal of Biomedical Science.

Missense mutation in LAMA3 associated with Herlitz Junctional Epidermolysis Bullosa in a Pakistani family.

A. Klausegger, J. Bauer, R. Qamar, 2012 .

A novel homozygous 62‐bp insertion in ECM1 causes lipoid proteinosis in a multigeneration Pakistani family

M. Ajmal, A. Hameed, M. Nasir, 2009, The British journal of dermatology.

Genetic associations of psoriasis in a Pakistani population

James T. Elder, P E Stuart, J. Voorhees, 2013, The British journal of dermatology.

IL-22 in hepatocyte’s survival of Pakistani patients with end stage liver disease: an insight into IL 22 mediated hepato-regenerative pathway

A. Latif, S. Manzoor, M. Saalim, 2019, Molecular Biology Reports.

Identification of recurrent c.742G>T nonsense mutation in ECM1 in Pakistani families suffering from lipoid proteinosis

S. Malik, A. Mir, N. Ahmad, 2014, Molecular Biology Reports.

In silico characterization of a novel pathogenic deletion mutation identified in XPA gene in a Pakistani family with severe xeroderma pigmentosum

S. Malik, N. Ahmad, A. Hameed, 2013, Journal of Biomedical Science.

IL-22 in hepatocyte’s survival of Pakistani patients with end stage liver disease: an insight into IL 22 mediated hepato-regenerative pathway

A. Latif, S. Manzoor, M. Saalim, 2019, Molecular Biology Reports.