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Year | Number of Results |
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2002 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (cited) for id: 618349
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Homozygous splicing mutation in NUP133 causes Galloway-Mowat syndrome.
Ann Neurol. 2018 Dec;84(6):814-828. doi: 10.1002/ana.25370.
Ann Neurol. 2018.
PMID: 30427554
Another autosomal recessive form of focal glomerulosclerosis with neurological findings.
Nakazato H, Hattori S, Karashima S, Kawano T, Seguchi S, Kanahori M, Endo F.
Nakazato H, et al.
Pediatr Nephrol. 2002 Jan;17(1):16-9. doi: 10.1007/s004670200003.
Pediatr Nephrol. 2002.
PMID: 11793129
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