Rare missense TUBGCP5 gene variant in a patient with primary microcephaly

Results

Naziv:	Rare missense TUBGCP5 gene variant in a patient with primary microcephaly
Autori:	Maver, Aleš; Čuturilo, Goran ; Kovanda, Anja; Miletić, Aleksandra; Peterlin, Borut
Godina:	2019
Publikacija:	European journal of medical genetics
ISSN:	1769-7212 European Journal of Medical Genetics Pretraži identifikator
Izdavač:	Amsterdam : Elsevier
Tip rezultata:	Naučni članak
Kolacija:	vol. 62 br. 12 str. 103598
DOI:	10.1016/j.ejmg.2018.12.003
WoS-ID:	000496913300013
Scopus-ID:	2-s2.0-85059132911
PMID:	30543990
URI:	https://enauka.gov.rs/handle/123456789/279594
URL:	https://www.sciencedirect.com/science/article/abs/pii/S176972121830274X?via%3Dihub
Izvor metapodataka:	Migrirano iz RIS podataka
M-kategorija:	22M22 - Međunarodni časopis kategorije M22

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