Cantu syndrome: Uncovering a rare gain-of-function ABCC9 gene mutation with possible therapeutic implications for the treatment of hypertrichosis

doi:10.1016/j.jaad.2016.02.662

Cantu syndrome: Uncovering a rare gain-of-function ABCC9 gene mutation with possible therapeutic implications for the treatment of hypertrichosis

https://doi.org/10.1016/j.jaad.2016.02.662

Copy DOI

Export

Save

Cite

Journal: Journal of the American Academy of Dermatology

Publication Date: Apr 20, 2016

#Cantu Syndrome #Treatment Of Hypertrichosis #ABCC9 Gene #Therapeutic Implications #Gene Mutation

Abstract
Full-Text
Similar Papers

Abstract

Listen

Cantu syndrome: Uncovering a rare gain-of-function ABCC9 gene mutation with possible therapeutic implications for the treatment of hypertrichosis

Full Text

Published Version

Check institute access

Open DOI Link

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Similar Papers

Paper Title

Journal

Date

Author

View more papers

More From: Journal of the American Academy of Dermatology

Paper Title

Journal

Date

Author

View more papers

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.

R Discovery Prime

Cantu syndrome: Uncovering a rare gain-of-function ABCC9 gene mutation with possible therapeutic implications for the treatment of hypertrichosis