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(1 - 6 of 6)
Analysis of shared heritability in common disorders of the brain
Anttila, V.; Bulik-Sullivan, B.; Finucane, H.K.; Walters, R.K.; Bras, J.; Duncan, L.; ... ; Zayats 2018
Analysis of shared heritability in common disorders of the brain
Article / Letter to editor
open access
PATIENTS AFFECTED BY MOSAIC PCDH19 MUTATIONS: 5 NEW CASES
Lange, I. de; Rump, P.; Neuteboom, R.; Augustijn, P.; Hodges, K.; Kistemaker, A.; ... ; Brilstra, E. 2017
PATIENTS AFFECTED BY MOSAIC PCDH19 MUTATIONS: 5 NEW CASES
Article / Letter to editor
metadata only
Male patients affected by mosaic PCDH19 mutations: five new cases
Lange, I.M. de; Rump, P.; Neuteboom, R.F.; Augustijn, P.B.; Hodges, K.; Kistemaker, A.I.; ... ; Brilstra, E.H. 2017
Male patients affected by mosaic PCDH19 mutations: five new cases
Article / Letter to editor
open access
Structural genomic variation in childhood epilepsies with complex phenotypes
Helbig, I.; Swinkels, M.E.M.; Aten, E.; Caliebe, A.; Slot, R. van 't; Boor, R.; ... ; Koeleman, B.P.C. 2014
Structural genomic variation in childhood epilepsies with complex phenotypes
Article / Letter to editor
metadata only
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling
Logan, C.V.; Szabadkai, G.; Sharpe, J.A.; Parry, D.A.; Torelli, S.; Childs, A.M.; ... ; UK10K Consortium 2014
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling
Article / Letter to editor
metadata only
RARE STRUCTURAL GENOMIC VARIANTS IN NONSYNDROMIC EPILEPTIC ENCEPHALOPATHIES WITH AND WITHOUT MRI- DETECTABLE STRUCTURAL BRAIN ABNORMALITIES
Helbig, I.; Swinkels, M.E.M.; Moller, R.S.; Aten, E.; Brilstra, E.H.; Ostertag, P.; ... ; Poot, M. 2010
RARE STRUCTURAL GENOMIC VARIANTS IN NONSYNDROMIC EPILEPTIC ENCEPHALOPATHIES WITH AND WITHOUT MRI- DETECTABLE STRUCTURAL BRAIN ABNORMALITIES
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