Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype

Harry Pachajoa, William Lopez-Quintero, Sara Vanegas, Claudia Montoya, Diana Ramírez-Montaño
  • The Application of Clinical Genetics, March 2018, Dove Medical Press
  • DOI: 10.2147/tacg.s155022

The authors haven't finished explaining this publication. If you are the author, sign in to claim or explain your work.

open access logoRead Publication

http://dx.doi.org/10.2147/tacg.s155022

The following have contributed to this page: William López and Claudia Montoya