Associated Papers
A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene.
Morikawa H et al.
Human Genome Variation, 2023
36964172 (PubMed )
Supplement: 41439_2023_239_MOESM1_ESM.xlsx › candidate_variants
Identification of a novel LATS1 variant associated with familial cerebral cavernous malformations in a Chinese family.
Geng L et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2022
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