论文信息 - Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma - 字舞流文

Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma

R. Mani | A. Anand | Arunima Chatterjee | R. Hiremagalore | Nishtha Pandey | B. Rajashekhar | Dennis F. Xavier | Ajith Tharakan | Ram-Shankar Mani