Wide clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2 gene

dc.contributor.author	Gooding, R.
dc.contributor.author	King, R. H. M.
dc.contributor.author	Angelicheva, D.
dc.contributor.author	Colomer, J.
dc.contributor.author	Parman, Y.
dc.contributor.author	Kalaydjieva, L.
dc.contributor.author	Conill, J.
dc.contributor.author	Nascimento, A.
dc.date.accessioned	2021-03-03T13:57:52Z
dc.date.available	2021-03-03T13:57:52Z
dc.identifier.citation	Colomer J., Gooding R., Angelicheva D., King R. H. M. , Parman Y., Nascimento A., Conill J., Kalaydjieva L., "Wide clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2 gene", 11th International Congress of the World-Muscle-Society, Brugge, Belçika, 4 - 07 Ekim 2006, cilt.16, ss.664-665
dc.identifier.other	av_370225e1-7171-4851-aaeb-0dc5d1c04d0c
dc.identifier.other	vv_1032021
dc.identifier.uri	http://hdl.handle.net/20.500.12627/41113
dc.identifier.uri	https://doi.org/10.1016/j.nmd.2006.05.078
dc.language.iso	eng
dc.subject	Nöroloji
dc.subject	Sinirbilim ve Davranış
dc.subject	Yaşam Bilimleri (LIFE)
dc.subject	Tıp
dc.subject	Sağlık Bilimleri
dc.subject	Dahili Tıp Bilimleri
dc.subject	Temel Bilimler
dc.subject	Yaşam Bilimleri
dc.subject	KLİNİK NEUROLOJİ
dc.subject	Klinik Tıp
dc.subject	Klinik Tıp (MED)
dc.subject	NEUROSCIENCES
dc.title	Wide clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2 gene
dc.type	Bildiri
dc.contributor.department	, ,
dc.identifier.volume	16
dc.contributor.firstauthorID	132839

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