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Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome
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- Liu, L (author)
- Karolinska Institutet
- Done, SC (author)
- Khoshnoodi, J (author)
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- Wartiovaara, J (author)
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- Oxford University Press (OUP), 2001
- 2001
- English.
- In: Human molecular genetics. - : Oxford University Press (OUP). - 0964-6906 .- 1460-2083. ; 10:23, s. 2637-2644
- Journal article (peer-reviewed)
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- Liu, L
- Done, SC
- Khoshnoodi, J
- Bertorello, A
- Wartiovaara, J
- Berggren, PO
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- Tryggvason, K
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