Skip to main content
Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Exons 1–3 deletion in FLCN is associated with increased risk of pneumothorax in Chinese patients with Birt-Hogg-Dubé syndrome

Fig. 1

Point mutations at FLCN found in our cohort are listed. White boxes represent exons and yellow boxes represent exons with pathogenic point mutations in FLCN. The number of patients for each mutation is given in parentheses. *One patient in each of the three mutations did not undergo genetic testing, but the mutations were identified in their first-degree relatives

Back to article page