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Congenital hepatic fibrosis and polycystic kidney disease not linked to C >A mutation in exon 29 of in a Persian cat
Case summary We describe the case of a 1-year-old male Persian cat diagnosed with congenital hepatic fibrosis (CHF) associated with renal polycystic disease and, for the first time, we have shown that there was no C >A mutation in exon 29 of PKD1 (polycystic kidney disease 1). The cat presented w...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
SAGE Publishing
2015-12-01
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| Serie: | Journal of Feline Medicine and Surgery Open Reports |
| Accesso online: | https://doi.org/10.1177/2055116915619191 |
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