Phenotypical spectrum of congenital myasthenic syndrome caused by mutations in COLQ gene

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Title:	Phenotypical spectrum of congenital myasthenic syndrome caused by mutations in COLQ gene
Authors :	Mihaylova, V.; Müller, J.; Vilchez, J.; Salih, M.; Kabiraj, M.; D'Amico, A.; Bertini, E.; Woelfle, J.; Schreiner, F.; Kurlemann, G.; Milić-Rašić, Vedrana M.; Siskova, D.; Colomer, J.; Herczegfalvi, A.; Fabriciova, K.; Weschke, B.; Scola, R.; Hoellen, F.; Schara, U.; Abicht, A.; Lochmueller, H.;
Issue Date:	2008
Publication:	Journal of neurology
ISSN:	0340-5354 Journal of Neurology Search Idenfier
Publisher:	BerlinHeidelbergNew York : Dr. Dietrich Steinkopff Verlag; Springer
Type:	Conference Paper
Collation:	vol. 255 br. 4 str. 609-611
DOI:	10.1007/s00415-008-0769-y
WoS-ID:	000255747000703
Scopus-ID:	2-s2.0-42549136048
VBS COBISS:	1025288629
URI:	https://plus.cobiss.net/cobiss/sr/sr/bib/1025288629#izum.si https://enauka.gov.rs/handle/123456789/646530
M-category:	Mp. category will be shown later

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