Compound Heterozygous Mutation in SGPL1 Causes Autosomal Recessive Charcot-Marie-Tooth Disease Type 2 in a Serbian Family

Atkinson, Derek; Asselbergs, B; De, Vriendt Els; Ooms, T; Estrada-Cuzcano, A; Nikodinovic, Jelena; Milic-Rasic, Vedrana M; Jordanova, Albena

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Title:	Compound Heterozygous Mutation in SGPL1 Causes Autosomal Recessive Charcot-Marie-Tooth Disease Type 2 in a Serbian Family
Authors:	Atkinson, Derek; Asselbergs, B; De, Vriendt Els; Ooms, T; Estrada-Cuzcano, A; Nikodinovic, Jelena; Milic-Rasic, Vedrana M; Jordanova, Albena
Issue Date:	2016
Publication:	JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
ISSN:	1085-9489 Journal of the Peripheral Nervous System Search Idenfier
Type:	Conference Paper
Collation:	vol. 21 br. 3 str. 233-233
WoS-ID:	000383856200213
URI:	https://enauka.gov.rs/handle/123456789/815351
Metadata source:	(Preuzeto iz Nasi u WoS)
M-category:	Mp. category will be shown later

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