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Browsing by Author Kamsteeg, EJ

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	Title	Author(s)	Issue Date
	A DYNC1H1 mutation causes a lower extremity predominance spinal muscular atrophy Proceeding/Conference:Annual Scientific Meeting of the Asian and Oceanian Myology Center, AOMC 2016	Chan, SHS Chung, BHY Mak, CCY Kamsteeg, EJ	2016
	Mutations in ATP6V1E1 or ATP6V1A cause autosomal-recessive cutis laxa Journal:American Journal of Human Genetics	van Damme, T Gardeitchik, T Mohamed, M Guerrero-Castillo, S Freisinger, P Guillemyn, B Kariminejad, A Dalloyaux, D van Kraaij, S Lefeber, DJ Syx, D Steyaert, W DeRycke, R Hoischen, A Kamsteeg, EJ Wong, SY van Scherpenzeel, M Jamali, P Brandt, P Nijtmans, L Korenke, GC Chung, BHY MAK, CCY Hausser, I Kornak, U Fischer-Zirnsak, B Strom, TM Meitinger, T Alanay, Y Utine, GE Leung, KCP Ghaderi-Sohi, S Coucke, P Symoens, S De Paepe, A Thiel, C Haack, TB Malfait, F Morava, E Callewaert, B Wevers, RA	2017
	Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service Journal:Journal of Neuromuscular Diseases	Westra, D Schouten, MI Stunnenberg, BC Kusters, B Saris, CGJ Erasmus, CE van Engelen, BG Bulk, S Verschuuren-Bemelmans, CC Gerkes, EH de Geus, C van der Zwaag, PA Chan, S Chung, B Barge-Schaapveld, DQCM Kriek, M Sznajer, Y van Spaendonck-Zwarts, K van der Kooi, AJ Krause, A Schonewolf-Greulich, B de Die-Smu8lders, C Sallevelt, SCEH Krapels, IPC Rasmussen, M Maystadt, I Kievit, AJA Witting, N Pennings, M Meijer, R Gillissen, C Kamsteeg, EJ Voermans, NC	2019

Showing results 1 to 3 of 3