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eNauka >  Results >  The clinical significance ofA2ML1variants in Noonan syndrome has to be reconsidered
Title: The clinical significance ofA2ML1variants in Noonan syndrome has to be reconsidered
Authors : Brinkmann, Julia; ...; Cuturilo, Goran; ...; (broj, koautora 25)
Issue Date: 2021
Publication: EUROPEAN JOURNAL OF HUMAN GENETICS
ISSN: 1018-4813 European Journal of Human Genetics Search Idenfier
Type: Article
Collation: vol. 29 br. 3 str. 524-527
DOI: 10.1038/s41431-020-00743-3
WoS-ID: 000580465900001
Scopus-ID: 2-s2.0-85092785516
PMID: 33082526
PMCID: PMC7940614
URI: https://enauka.gov.rs/handle/123456789/797001
Project: ERN-ITHACA networking
German Federal Ministry of Education and Research-BMBF (German Network for RASopathy Research "GeNeRARe") [FKZ: 01GM1519A]
German Federal Ministry of Education and Research-BMBF (European Joint Programme on Rare Diseases (NSEuroNet
Metadata source: (Preuzeto iz Nasi u WoS)
M-category: 
21M21

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