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A study of new NEK8 mutations in patients with severe renal cystic hypodysplasia and ciliopathy-associated defects

2015-01-01

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Literature Corpus work: fe592939-40f1-5361-bedf-8ad6c7df6acb
DOI: 10.1186/2046-2530-4-s1-p54
PMCID: PMC4519170

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