Visualitza VHIR - Articles científics per autor "Abulí Vidal, Anna"
Ara mostrant els elements 1-4 d 4
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A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome
Keraite, Ieva; Becker, Philipp; Canevazzi, Davide; Frías-López, Cristina; Dabad, Marc; Tonda, Raul; Leno Colorado, Jorge; Abulí Vidal, Anna; García Arumí, Elena (Nature Portfolio, 2022-10-06) -
Intrafamilial variability in SLC6A1-related neurodevelopmental disorders
Kassabian, Benedetta; Fenger, Christina Dühring; Willems, Marjolaine; Aledo-Serrano, Angel; Linnankivi, Tarja; McDonnell, Pamela Pojomovsky; Abulí Vidal, Anna (Frontiers Media, 2023-07-12) -
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis
Stefanski, Arthur; Pérez-Palma, Eduardo; Brünger, Tobias; MONTANUCCI, LUDOVICA; Gati, Cornelius; Klöckner, Chiara; Abulí Vidal, Anna (Oxford University Press, 2023-12) -
The phenotypic presentation of adult individuals with SLC6A1-related neurodevelopmental disorders
Johannesen, Katrine M; Nielsen, Jimmi; Sabers, Anne; Isidor, Bertrand; Kattentidt-Mouravieva, Anja A.; Zieglgänsberger, Dominik; Abulí Vidal, Anna (Frontiers Media, 2023-08-17)