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CODAS Syndrome Is Associated with Mutations of LONP1, Encoding Mitochondrial AAA+ Lon Protease
Strauss, Kevin A., Jinks, Robert N., Puffenberger, Erik G., Venkatesh, Sundararajan, Singh, Kamalendra, Cheng, Iteen, Mikita, Natalie, Thilagavathi, Jayapalraja, Lee, Jae, Sarafianos, Stefan, Benkert,Volume:
96
Langue:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2014.12.003
Date:
January, 2015
Fichier:
PDF, 2.49 MB
english, 2015