Reactome | CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease

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CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease Show undefined attributes

author	[Person:9839293] Strauss, KA [Person:9839294] Jinks, RN [Person:9839289] Puffenberger, EG [Person:9838268] Venkatesh, S [Person:9682633] Singh, K [Person:9839285] Cheng, I [Person:9839288] Mikita, N [Person:9839268] Thilagavathi, J [Person:6790257] Lee, J [Person:9839295] Sarafianos, S [Person:9839282] Benkert, A [Person:9839287] Koehler, A [Person:9839257] Zhu, A [Person:9839256] Trovillion, V [Person:9839283] McGlincy, M [Person:9839284] Morlet, T [Person:9839254] Deardorff, M [Person:9839272] Innes, AM [Person:8875826] Prasad, C [Person:9839265] Chudley, AE [Person:9839264] Lee, IN [Person:9837984] Suzuki, CK
created	[InstanceEdit:9839255] May, Bruce, 2023-07-05
dbId	9839258
displayName	CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease
journal	Am J Hum Genet
pages	121-35
pubMedIdentifier	25574826
schemaClass	LiteratureReference
title	CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease
url	http://www.ncbi.nlm.nih.gov/pubmed/25574826
volume	96
year	2015

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[Summation:9838043] ATP hydrolysis drives translocation of the substrate protein...

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