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

✍ Scribed by Hameed, A.; Mir, A.; Nasir, M.; Ajmal, M.

• Book ID: 126463798
• Publisher: John Wiley and Sons
• Year: 2014
• Tongue: English
• Weight: 102 KB
• Volume: 87
• Category: Article
• ISSN: 0009-9163
• DOI: 10.1111/cge.12486