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

Autor: Pandey, Nishtha1,2, Xavier, Dennis F.3, Chatterjee, Arunima1, Mani, Ram‐Shankar1, Hiremagalore, Ravi4, Tharakan, Ajith5, Rajashekhar, B.3, Anand, Anuranjan1
Zdroj: Annals of Human Genetics. Jan2016, Vol. 80 Issue 1, p11-19. 9p.
Databáze: Academic Search Ultimate
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