Infantile peripheral neuropathy, deafness, and proximal tubulopathy associated with a novel mutation of the RRM2B gene: case study

Stojanovic, Vesna D; Mayr, Johannes A; Sperl, Wolfgang; Barisic, Nenad A; Doronjski, Aleksandra R; Milak, Gordana

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eNauka > Results > Infantile peripheral neuropathy, deafness, and proximal tubulopathy associated with a novel mutation of the RRM2B gene: case study

Title:	Infantile peripheral neuropathy, deafness, and proximal tubulopathy associated with a novel mutation of the RRM2B gene: case study
Authors:	Stojanovic, Vesna D ; Mayr, Johannes A; Sperl, Wolfgang; Barisic, Nenad A ; Doronjski, Aleksandra R; Milak, Gordana
Issue Date:	2013
Publication:	CROATIAN MEDICAL JOURNAL
ISSN:	0353-9504 Croatian Medical Journal Search Idenfier
Type:	Article
Collation:	vol. 54 br. 6 str. 579-584
DOI:	10.3325/cmj.2013.54.579
WoS-ID:	000329826800011
Scopus-ID:	2-s2.0-84892383403
PMID:	24382854
PMCID:	PMC3893987
URI:	https://enauka.gov.rs/handle/123456789/831626
Metadata source:	(Preuzeto iz Nasi u WoS)
M-category:	22M22

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