DDX39 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "DDX39" in English language version.

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doi.org (Global: 2^nd place; English: 2^nd place)

Peelman LJ, Chardon P, Nunes M, Renard C, Geffrotin C, Vaiman M, Van Zeveren A, Coppieters W, van de Weghe A, Bouquet Y, et al. (Aug 1995). "The BAT1 gene in the MHC encodes an evolutionarily conserved putative nuclear RNA helicase of the DEAD family". Genomics. 26 (2): 210–8. doi:10.1016/0888-7543(95)80203-X. PMID 7601445.
Treat K, Jangam S, Yamamoto S, White K, Kanca O, Christensen C, Lynch S, Baptista J, Tsang MH, Jay K, Chung BH, Yuen LY, Chui MM, Bellen H, Wangler M (2022-03-01). "eP410: De novo missense variants in DDX39B cause a novel syndrome characterized by neurodevelopmental delay, short stature and congenital hypotonia". Genetics in Medicine. 2022 ACMG Annual Clinical Genetics Meeting. 24 (3, Supplement): S257 – S258. doi:10.1016/j.gim.2022.01.445. ISSN 1098-3600.

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: DDX39 DEAD (Asp-Glu-Ala-Asp) box polypeptide 39".

Peelman LJ, Chardon P, Nunes M, Renard C, Geffrotin C, Vaiman M, Van Zeveren A, Coppieters W, van de Weghe A, Bouquet Y, et al. (Aug 1995). "The BAT1 gene in the MHC encodes an evolutionarily conserved putative nuclear RNA helicase of the DEAD family". Genomics. 26 (2): 210–8. doi:10.1016/0888-7543(95)80203-X. PMID 7601445.

Treat K, Jangam S, Yamamoto S, White K, Kanca O, Christensen C, Lynch S, Baptista J, Tsang MH, Jay K, Chung BH, Yuen LY, Chui MM, Bellen H, Wangler M (2022-03-01). "eP410: De novo missense variants in DDX39B cause a novel syndrome characterized by neurodevelopmental delay, short stature and congenital hypotonia". Genetics in Medicine. 2022 ACMG Annual Clinical Genetics Meeting. 24 (3, Supplement): S257 – S258. doi:10.1016/j.gim.2022.01.445. ISSN 1098-3600.

Treat K, Jangam S, Yamamoto S, White K, Kanca O, Christensen C, Lynch S, Baptista J, Tsang MH, Jay K, Chung BH, Yuen LY, Chui MM, Bellen H, Wangler M (2022-03-01). "eP410: De novo missense variants in DDX39B cause a novel syndrome characterized by neurodevelopmental delay, short stature and congenital hypotonia". Genetics in Medicine. 2022 ACMG Annual Clinical Genetics Meeting. 24 (3, Supplement): S257 – S258. doi:10.1016/j.gim.2022.01.445. ISSN 1098-3600.