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American Journal of Human Genetics|November 22, 2022
A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanismShridhar Parthasarathy, Sarah McKeown Ruggiero, Antoinette Gelot, et al.Plos One|March 2, 2011
The genomic ancestry of individuals from different geographical regions of Brazil is more uniform than expectedSérgio D J Pena, Giuliano Di Pietro, Mateus Fuchshuber-Moraes, et al.Forensic Science International|July 5, 2003
The 2000-2001 GEP-ISFG Collaborative Exercise on mtDNA: assessing the cause of unsuccessful mtDNA PCR amplification of hair shaft samplesLourdes Prieto, Marta Montesino, Antonio Salas, et al.Current Biology : CB|December 3, 2014
Two ancient human genomes reveal Polynesian ancestry among the indigenous Botocudos of BrazilAnna-Sapfo Malaspinas, Oscar Lao, Hannes Schroeder, et al.Neurology|July 2, 2017
<i>DNM1</i> encephalopathy: A new disease of vesicle fissionSarah von Spiczak, Katherine L Helbig, Deepali N Shinde, et al.Brain : a Journal of Neurology|October 21, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathiesSilvia Masnada, Ulrike B S Hedrich, Elena Gardella, et al.Journal of Bacteriology|August 4, 2005
Swine and poultry pathogens: the complete genome sequences of two strains of Mycoplasma hyopneumoniae and a strain of Mycoplasma synoviaeAna Tereza R Vasconcelos, Henrique B Ferreira, Cristiano V Bizarro, et al.Pageof 10