Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.
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Lahrouchi N, et al. Among authors: george a.
Nat Commun. 2019 Mar 12;10(1):1180. doi: 10.1038/s41467-019-08547-w.
Nat Commun. 2019.
PMID: 30862798
Free PMC article.