Intronic splicing mutations in PTCH1 cause Gorlin syndrome

Authors

Keywords

Gorlin syndrome, Familial BCC, Deep intronic splicing mutations, Nevoid basal cell carcinoma syndrome (NBCCS), <em class=EmphasisTypeItalic >PTCH1</em>

Journal

Familial Cancer

Volume 13, Issue 3, Pages 477-480

Publisher

Springer Nature

Online

2014-03-21

DOI

10.1007/s10689-014-9712-9

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