Structure and function of the cystic fibrosis transmembrane conductance regulator

Cystic fibrosis (CF) is a lethal autosomal recessive genetic disease caused by mutations in the CF transmembrane conductance regulator (CFTR). Mutations in the CFTR gene may result in a defective processing of its protein and alter the function and regulation of this channel. Mutations are associate...

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Principais autores:	M.M. Morales, M.A.M. Capella, A.G. Lopes
格式:	Artigo
語言:	Inglês
出版:	Associação Brasileira de Divulgação Científica 1999-08-01
叢編:	Brazilian Journal of Medical and Biological Research
主題:	CFTR cystic fibrosis chloride channel function structure mutations
在線閱讀:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999000800013
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