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Author/Creator Chow, Chung W.

1. Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5. (12th March 2015)

Authors:
Scerri, Thomas; Riseley, Jessica R.; Gillies, Greta; Pope, Kate; Burgess, Rosemary; Mandelstam, Simone A.; Dibbens, Leanne; Chow, Chung W.; Maixner, Wirginia; Harvey, Anthony Simon; Jackson, Graeme D.; Amor, David J.; Delatycki, Martin B.; Crino, Peter B.; Berkovic, Samuel F.; Scheffer, Ingrid E....
Journal:
Annals of clinical and translational neurology
Issue:
Volume 2:Number 5(2015:May)
Page Start:
575
Record Type:
Journal Article
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3. Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility. Issue 3 (6th February 2014)

Authors:
Leventer, Richard J.; Jansen, Floor E.; Mandelstam, Simone A.; Ho, Alice; Mohamed, Ismail; Sarnat, Harvey B.; Kato, Mitsuhiro; Fukasawa, Tatsuya; Saitsu, Hirotomo; Matsumoto, Naomichi; Itoh, Masayuki; Kalnins, Renate M.; Chow, Chung W.; Harvey, A. Simon; Jackson, Graeme D.; Crino, Peter B.; Berko...
Journal:
Epilepsia
Issue:
Volume 55:Issue 3(2014:Mar.)
Page Start:
e22
Record Type:
Journal Article
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5. Neuropathology of childhood‐onset basal ganglia degeneration caused by mutation of VAC14. Issue 12 (7th November 2017)

Authors:
Stutterd, Chloe; Diakumis, Peter; Bahlo, Melanie; Fanjul Fernandez, Miriam; Leventer, Richard J.; Delatycki, Martin; Amor, David; Chow, Chung W.; Stephenson, Sarah; Meisler, Miriam H.; Mclean, Catriona; Lockhart, Paul J.
Journal:
Annals of clinical and translational neurology
Issue:
Volume 4:Issue 12(2017)
Page Start:
859
Record Type:
Journal Article
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