Found: 5
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High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients.
- Published in:
- Nephrology, 2016, v. 21, n. 3, p. 209, doi. 10.1111/nep.12563
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- Publication type:
- Article
Clinical features and mutation of NPHP5 in two Chinese siblings with Senior- Løken syndrome.
- Published in:
- Nephrology, 2013, v. 18, n. 12, p. 838, doi. 10.1111/nep.12156
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- Publication type:
- Article
Podocyte-specific Nup160 knockout mice develop nephrotic syndrome and glomerulosclerosis.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 8, p. 667, doi. 10.1093/hmg/ddad211
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- Publication type:
- Article
Novel Mutation of OCRL1 in Lowe Syndrome.
- Published in:
- Indian Journal of Pediatrics, 2015, v. 82, n. 1, p. 89, doi. 10.1007/s12098-014-1581-6
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- Publication type:
- Article
Scalp Tumor and Hydroureteronephrosis in Patients with Nephronophthisis and Homozygous NPHP1 Deletion.
- Published in:
- Clinical Pediatrics, 2023, v. 62, n. 12, p. 1508, doi. 10.1177/00099228231162416
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- Publication type:
- Article