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High mutation detection rates in cerebral cavernous malform..:

Spiegler, Stefanie ; Najm, Juliane ; Liu, Jian...
Molecular Genetics & Genomic Medicine. 2 (2014) 2 - p. 176-185 , 2014

RT Journal
T1 <Title>High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one‐third of probands are minors</Title>

UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_mgg3.60&Exemplar=1&LAN=DE
				
A1 Spiegler, Stefanie
A1 Najm, Juliane
A1 Liu, Jian
A1 Gkalympoudis, Stephanie
A1 Schröder, Winnie
A1 Borck, Guntram
A1 Brockmann, Knut
A1 Elbracht, Miriam
A1 Fauth, Christine
A1 Ferbert, Andreas
A1 Freudenberg, Leonie
A1 Grasshoff, Ute
A1 Hellenbroich, Yorck
A1 Henn, Wolfram
A1 Hoffjan, Sabine
A1 Hüning, Irina
A1 Korenke, G. Christoph
A1 Kroisel, Peter M.
A1 Kunstmann, Erdmute
A1 Mair, Martina
A1 Munk‐Schulenburg, Susanne
A1 Nikoubashman, Omid
A1 Pauli, Silke
A1 Rudnik‐Schöneborn, Sabine
A1 Sudholt, Irene
A1 Sure, Ulrich
A1 Tinschert, Sigrid
A1 Wiednig, Michaela
A1 Zoll, Barbara
A1 Ginsberg, Mark H.
PB Wiley
YR 2014
SN 2324-9269
SN 2324-9269
JF Molecular Genetics & Genomic Medicine
VO 2
IS 2
SP 176
OP 185
LK http://dx.doi.org/https://doi.org/10.1002/mgg3.60
DO https://doi.org/10.1002/mgg3.60
SF ELIB - SuUB Bremen

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