Bioinformatics evaluation of NPHS2 deletion mutation associated with congenital nephrotic syndrome in a consanguineous Pakistani family

Publisher: John Wiley & Sons Inc

E-ISSN: 1399-0004|87|6|599-601

ISSN: 0009-9163

Source: CLINICAL GENETICS, Vol.87, Iss.6, 2015-06, pp. : 599-601

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