Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits1
- Authors
- Lynn MCKEOWN
- Philip ROBINSON
- Owen T JONES
- Lacinova L.
- Autret L
- Weick JP
- Fox AP
- Yaari Y
- Catterall WA
- Williams ME
- Jones OT
- Mills LR
- Elliott EM
- Westenbroek RE
- Garcia J
- Chaudhari N.
- Jurkat-Rott K
- Elbaz A
- Monnier N
- Sipos I
- Lehmann-Horn F
- Zhang Z
- Seino S
- Matthes J
- Mangoni ME
- Dou H
- Bech-Hansen NT
- Zeitz C
- Matsushita K
- Qian J
- Wu LG
- Llinas RR
- Noebels JL
- Zwingman TA
- Mori Y
- Tsuji S
- Lorenzon NM
- Dove LS
- Qian J
- Matsushita K
- Caddick SJ
- Zhou YD
- Eunson LH
- Imbrici P
- Trettel F
- Ishikawa K
- Chioza B
- Jouvenceau A
- Strupp M
- Saegusa H
- Ino M
- Kamp MA
- Saegusa H
- Jing X
- Yunker AM
- Mizuta E
- Anderson MP
- Mangoni ME
- Cribbs LL
- Bourinet E
- Stamboulian S
- Khosravani H
- Talley EM
- Perez-Reyes E.
- Wan J
- Hoda JC
- Hoda JC
- Battistini S
- Vahedi K
- Carrera P
- Gardner K.
- Denier C
- Wiser O
- Publication date
- Publisher
- 'Wiley'
- Doi
Abstract
Abstract is not available.Similar works
This paper was published in Crossref.
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