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1 Ergebnisse
1
Exome sequencing identifies a novel TRPV4 mutation in a CMT..:
Landouré, Guida
;
Sullivan, Jeremy M.
;
Johnson, Janel O.
...
Neurology. 79 (2012) 2 - p. 192-194 , 2012
Link:
https://doi.org/10.1212/wnl.0b013e31825f04b2
RT Journal T1
Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family
UL https://suche.suub.uni-bremen.de/peid=cr-10.1212_wnl.0b013e31825f04b2&Exemplar=1&LAN=DE A1 Landouré, Guida A1 Sullivan, Jeremy M. A1 Johnson, Janel O. A1 Munns, Clare H. A1 Shi, Yijun A1 Diallo, Oumarou A1 Gibbs, J. Raphael A1 Gaudet, Rachelle A1 Ludlow, Christy L. A1 Fischbeck, Kenneth H. A1 Traynor, Bryan J. A1 Burnett, Barrington G. A1 Sumner, Charlotte J. PB Ovid Technologies (Wolters Kluwer Health) YR 2012 SN 0028-3878 SN 1526-632X JF Neurology VO 79 IS 2 SP 192 OP 194 LK http://dx.doi.org/https://doi.org/10.1212/wnl.0b013e31825f04b2 DO https://doi.org/10.1212/wnl.0b013e31825f04b2 SF ELIB - SuUB Bremen
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