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Association of a 3-Amino Acid Deletion Mutation of NPHS2 gene with Congenital Nephrotic Syndrome (CNS) in a consanguineo

Association of a 3-Amino Acid Deletion Mutation of NPHS2 gene with Congenital Nephrotic Syndrome (CNS) in a consanguineous Pakistani family. Muhammad Ajmal, Muhammad Nasir and Abdul Hameed Institute of Biomedical and Genetic Engineering 24-Mauve Area, G-9/1 Islamabad. Introduction.

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