NTNG1 mutations are a rare cause of Rett syndrome
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Published in American journal of medical genetics. Part A (01.04.2006)
Published in American journal of medical genetics. Part A (01.04.2006)
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Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A
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Published in The Journal of experimental medicine (04.10.2021)
Published in The Journal of experimental medicine (04.10.2021)
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Journal Article
Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A
Lepelley, Alice, Erika Della Mina, Erika Van Nieuwenhove, Waumans, Lise, Fraitag, Sylvie, Rice, Gilian I, Dhir, Ashish, Marie-Louise Frémond, Rodero, Mathieu P, Seabra, Luis, Carter, Edwin, Bodemer, Christine, Buhas, Daniela, Callewaert, Bert, De Lonlay, Pascale, Lien De Somer, Dyment, David A, Faes, Fran, Grove, Lucy, Holden, Simon, Hully, Marie, Kurian, Manju A, Mcmillan, Hugh J, Suetens, Kristin, Tyynismaa, Henna, Chhun, Stéphanie, Wai, Timothy, Wouters, Carine, Bader-Meunier, Brigitte, Crow, Yanick J
Published in bioRxiv (03.04.2021)
Published in bioRxiv (03.04.2021)
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Paper
VORSEHEN EINER OPTIMIERTEN SCHRITTMACHERFREQUENZ, DIE MIT DEN PHYSIOLOGISCHEN ERFORDERNISSEN DES PATIENTEN VARIIERT
NICHOLS, LUCY, M., MAPLE GROVE, MN 55369, US, ROLINE, GLENN, M., ANOKA, MN 55303, US, THOMPSON, DAVID, L., FRIDLEY, MN 55432, US, BENNETT, TOMMY, D., SHOREVIEW, MN 55126, US
Year of Publication 18.09.1997
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Year of Publication 18.09.1997
Patent