A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features.
Murata Y, Kurosaka H, Ohata Y, Aikawa T, Takahata S, Fujii K, Miyashita T, Morita C, Inubushi T, Kubota T, Sakai N, Ozono K, Kogo M, Yamashiro T.
Murata Y, et al. Among authors: kogo m.
Hum Genome Var. 2019 Apr 2;6:16. doi: 10.1038/s41439-019-0047-9. eCollection 2019.
Hum Genome Var. 2019.
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Free PMC article.