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ArticleGenetics in medicine : official journal of the American College of Medical Genetics2025

Bi-allelic loss-of-function variants in POC5 cause a syndromic retinal, endocrine, and neuromuscular ciliopathy.

Anneke T Vulto-van Silfhout et al.PubMed ↗Full text ↗Publisher ↗

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2 papers cite it

2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 40590205