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Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability
| Title: | Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability | Authors  : | Kroll-Hermi, Ariane; ...; Cuturilo, Goran; ...; (broj, koautora 89) | Issue Date: | 2025 | Publication: | AMERICAN JOURNAL OF HUMAN GENETICS | ISSN: | 0002-9297 American Journal of Human Genetics Search Idenfier |
Type: | Article | Collation: | vol. 112 br. 12 str. 2943-2960 | DOI: | 10.1016/j.ajhg.2025.10.014 | WoS-ID: | 001652221600001 | Scopus-ID: | 2-s2.0-105023389271 | URI: | https://enauka.gov.rs/handle/123456789/1029097 | Metadata source: | (Preuzeto iz Nasi u WoS) | M-category: | 21a+M21a+ |
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