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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
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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