Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma

Figure S1. A heterozygous single base substitution in GJB6 (c.31G>A; p.Gly11Arg) in the patient and her mother (arrows). Figure S2. A heterozygous single base substitution in GJB2 (c.109G>A; p.Val37Ile) in the patient, her mother, and a normal control (arrows). Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.