Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype
Harry Pachajoa,1,2 William López-Quintero,3 Sara Vanegas,1 Claudia L Montoya,3 Diana Ramírez-Montaño1 1Department of Basic Medical Sciences, Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Universidad Icesi, Cali, Valle del Cauca, Colombia; 2P...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Dove Medical Press
2018-03-01
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Series: | The Application of Clinical Genetics |
Subjects: | |
Online Access: | https://www.dovepress.com/novel-mutation-in-abbc9-gene-associated-with-congenital-hypertrichosis-peer-reviewed-article-TACG |