Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders.

Autor:	Mannucci, Ilaria1 (AUTHOR), Dang, Nghi D. P.2 (AUTHOR), Huber, Hannes3 (AUTHOR), Murry, Jaclyn B.4,5 (AUTHOR), Abramson, Jeff6 (AUTHOR), Althoff, Thorsten6 (AUTHOR), Banka, Siddharth7,8 (AUTHOR), Baynam, Gareth9,10,11 (AUTHOR), Bearden, David12 (AUTHOR), Beleza-Meireles, Ana13 (AUTHOR), Benke, Paul J.14 (AUTHOR), Berland, Siren15 (AUTHOR), Bierhals, Tatjana1 (AUTHOR), Bilan, Frederic16,17 (AUTHOR), Bindoff, Laurence A.18,19 (AUTHOR), Braathen, Geir Julius20 (AUTHOR), Busk, Øyvind L.20 (AUTHOR), Chenbhanich, Jirat21 (AUTHOR), Denecke, Jonas22 (AUTHOR), Escobar, Luis F.23 (AUTHOR)
Zdroj:	Genome Medicine. 6/7/2021, Vol. 13 Issue 1, p1-19. 19p.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu