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eNauka >  Rezultati >  N-terminal RAG1 frameshift mutations in Omenn's syndrome: Internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domains
Naziv: N-terminal RAG1 frameshift mutations in Omenn's syndrome: Internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domains
Autori: Santagata, S; Gomez, CA; Sobacchi, Cristina; Bozzi, F; Abinun, Mario; Pasic, Srdjan S; Cortes, P; Vezzoni, P; Villa, A
Godina: 2000
Publikacija: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN: 0027-8424 Proceedings of the National Academy of Sciences of the United States Pretraži identifikator
Tip rezultata: Naučni članak
Kolacija: vol. 97 br. 26 str. 14572-14577
DOI: 10.1073/pnas.97.26.14572
WoS-ID: 000165993700105
Scopus-ID: 2-s2.0-0034687695
PMID: 11121059
PMCID: PMC18960
URI: https://enauka.gov.rs/handle/123456789/820635
Izvor metapodataka: (Preuzeto iz Nasi u WoS)
M-kategorija: 
21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+

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