Téloméropathie (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Téloméropathie" in French language version.

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6,325^th place

634^th place

1aplasiemedullaire.com

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1telomero-asso.fr

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4,380^th place

low place

1oxfordjournals.org

1,389^th place

508^th place

1hematologylibrary.org

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3,702^nd place

1,293^rd place

405^th place

234^th place

147^th place

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3,952^nd place

aplasiemedullaire.com

« LIVRETS PATIENT », sur MaRIH FILIERE SANTE (consulté le 15 février 2023).

cshlp.org

rnajournal.cshlp.org

Trahan C1, Dragon F. Dyskeratosis congenita mutations in the H/ACA domain of human telomerase RNA affect its assembly into a pre-RNP, RNA, 2009;15:235-43

ens.fr

planet-vie.ens.fr

« Télomères et téloméropathies », sur Planet-Vie (consulté le 15 février 2023).

hematologylibrary.org

asheducationbook.hematologylibrary.org

Dokal I, Dyskeratosis congenita, Hematology Am Soc Hematol Educ Program, 2011;2011:480–486

jci.org

Tummala H, Walne A, Collopy L et al. Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita, J Clin Invest, 2015;125:2151-2160

nature.com

Heiss NS, Knight SW, Vulliamy TJ, Klauck SM, Wiemann S, Mason PJ, Poustka A, Dokal I. X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions, Nat Genet, 1998;1932-8

omim.org

Héritage mendélien chez l'Homme (en) 305000

oxfordjournals.org

hmg.oxfordjournals.org

Walne AJ, Vulliamy T, Marrone A et al. Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10, Hum Mol Genet, 2007;16:1619-29

pnas.org

Vulliamy T, Beswick R, Kirwan M, Marrone A, Digweed M, Walne A, Dokal I, Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita, Proc Natl Acad Sci U S A, 2008;105:8073-8

telomero-asso.fr

« Comprendre la maladie | TELOMERO ASSO », sur AssoConnect (consulté le 15 février 2023).