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Details on Person COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Class:IdLiteratureReference:2162291
_displayNameCOQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
_timestamp2012-03-19 14:16:29
author[Person:2162316] Heeringa, SF
[Person:2162325] Chernin, G
[Person:2162295] Chaki, M
[Person:1251976] Zhou, W
[Person:452788] Sloan, AJ
[Person:2162314] Ji, Z
[Person:2162312] Xie, LX
[Person:2162323] Salviati, L
[Person:432834] Hurd, TW
[Person:2162305] Vega-Warner, V
[Person:2162301] Killen, PD
[Person:444437] Raphael, Y
[Person:2162280] Ashraf, S
[Person:2162324] Ovunc, B
[Person:2162321] Schoeb, DS
[Person:2162336] McLaughlin, HM
[Person:2162342] Airik, R
[Person:2162307] Vlangos, CN
[Person:2162313] Gbadegesin, R
[Person:2162284] Hinkes, B
[Person:2162296] Saisawat, P
[Person:2162317] Trevisson, E
[Person:2162319] Doimo, M
[Person:2162338] Casarin, A
[Person:2162315] Pertegato, V
[Person:2162334] Giorgi, G
[Person:196832] Prokisch, H
[Person:2162331] Rötig, A
[Person:1971498] Nürnberg, G
[Person:452441] Becker, C
[Person:140991] Wang, S
[Person:2162281] Ozaltin, F
[Person:2162341] Topaloglu, R
[Person:2162302] Bakkaloglu, A
[Person:2162285] Bakkaloglu, SA
[Person:2162340] Müller, D
[Person:2162329] Beissert, A
[Person:2162318] Mir, S
[Person:2162299] Berdeli, A
[Person:2162339] Varpizen, S
[Person:937357] Zenker, M
[Person:2162298] Matejas, V
[Person:2162282] Santos-Ocaña, C
[Person:2162309] Navas, P
[Person:2162290] Kusakabe, T
[Person:207158] Kispert, A
[Person:917822] Akman, S
[Person:2162326] Soliman, NA
[Person:2162343] Krick, S
[Person:373425] Mundel, P
[Person:373556] Reiser, J
[Person:1971451] Nürnberg, P
[Person:2162304] Clarke, CF
[Person:654762] Wiggins, RC
[Person:373402] Faul, C
[Person:2162333] Hildebrandt, F
created[InstanceEdit:2162311] Williams, MG, 2012-03-19
journalJ Clin Invest
modified[InstanceEdit:2162344] Williams, MG, 2012-03-19
pages2013-24
pubMedIdentifier21540551
titleCOQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
volume121
year2011
(literatureReference)[Reaction:2162187] COQ6 hydroxylates DHB [Homo sapiens]
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No pathways have been reviewed or authored by COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness (2162291)