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

Authors Pachajoa H, López-Quintero W, Vanegas S, Montoya CL, Ramírez-Montaño D

Received 5 April 2018

Accepted for publication 5 April 2018

Published 31 May 2018 Volume 2018:11 Pages 75—76

DOI https://doi.org/10.2147/TACG.S170250


Pachajoa H, López-Quintero W, Vanegas S, Montoya CL, Ramírez-Montaño D. The Application of Clinical Genetics. 2018;11:15–21.

In the main title (page 15) and in the first column, third row of Table 1 (page 17), the gene name ABBC9 should be ABCC9.

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