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Neurogenetics|May 24, 2023
Aberrant Splicing Caused by a Novel VPS16 Variant Linked to Dystonia Type 30Mariana Santos, João Massano, Alexandra Manuel Lopes, et al.
Andrology|March 30, 2021
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohortMiriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, et al.
Andrology|June 26, 2022
Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertilityMiriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jiménez, et al.
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