Human PEX19: cDNA Cloning by Functional Complementation, Mutation Analysis in a Patient with Zellweger Syndrome, and Potential Role in Peroxisomal Membrane Assembly

Autor:	Matsuzono, Yuji, Kinoshita, Naohiko, Tamura, Shigehiko, Shimozawa, Nobuyuki, Hamasaki, Maho, Ghaedi, Kamran, Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Zdroj:	Proceedings of the National Academy of Sciences of the United States of America, 1999 Mar 01. 96(5), 2116-2121.
Databáze:	JSTOR Journals
Externí odkaz:	https://www.jstor.org/stable/47023 Zobrazit plný text záznamu