Servicio
Unidade de investigación
Publicacións (6) Publicacións nas que participase algún/ha investigador/a
2019
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A note on rotigotine for restless legs syndrome after renal transplantation
Movement Disorders
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Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria (PLoS Genet (2018) 14:12 (e1007813) DOI: )10.1371/journal.pgen.1007813
PLoS Genetics
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Erratum: Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019) 104(4) (767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001))
American Journal of Human Genetics
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Reply: Revisiting Genome Sequencing Data in Light of Novel Disease Gene Associations
Journal of the American College of Cardiology
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Response by Sheikh et al to Letter Regarding Article, "diagnostic Yield of Genetic Testing in Young Athletes with T-Wave Inversion"
Circulation
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Two Novel Cases of Autosomal Recessive Noonan Syndrome Associated With LZTR1 Variants
Revista Espanola de Cardiologia