Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/27/1/80/22869302/ddx386.pdf
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3. How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?;Brain Res,2012
4. Molecular genetics of X-linked Charcot-Marie-Tooth disease;Neuromolecular Med,2006
5. Connexin mutations in X-linked Charcot-Marie-Tooth disease;Science,1993
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