SASH1 is involved in an autosomal dominant lentiginous phenotype

Yiqun G. Shellman, Karoline A. Lambert, Anne Brauweiler, Pamela Fain, Richard A. Spritz, Melanie Martini, Klaus Peter Janssen, Neil F. Box, Tamara Terzian, Marian Rewers, Anelia Horvath, Constantine A. Stratakis, William A. Robinson, Steven E. Robinson, David A. Norris, Kristin B. Artinger, Theresa R. Pacheco

Research output: Contribution to journalLetterpeer-review

22 Scopus citations
Original languageEnglish (US)
Pages (from-to)3192-3194
Number of pages3
JournalJournal of Investigative Dermatology
Volume135
Issue number12
DOIs
StatePublished - Dec 1 2015
Externally publishedYes

Bibliographical note

Funding Information:
This research was supported by funds NIH/NIAMS K23AR49214 (to TRP), R03AR064555 (to YGS), P30AR057212 (to DAN/TRP/YGS/KBA), T32AR007411 (to AB), and Academic Enrichment Funds from the University of Colorado School of Medicine. The authors thank James Fitzpatrick for dermatopathologic interpretation of skin sections, Dr Christopher Korch at the University of Colorado DNA Sequencing Core (supported by NIH P30CA046934) for technical advice, and the University of Colorado Skin Cancer Biorepository for providing DNA samples.

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