[RYR1 myopathies in childhood: phenotype-genotype correlation and incidence]. [PDF]
Rev NeurolDel Arco-Guzmán N +5 more
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[Neurodevelopmental and Movement Disorder Due to a Mutation in the GNAO1 Gene: A Case Report]. [PDF]
Rev NeurolHernández Yeneris SM +4 more
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Chronic mucocutaneous candidiasis, mycobacterial infections and rosacea in a Mexican adult with STAT1 gain of function [PDF]
BiomedicaValerio-Gómez V +8 more
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Identification of a variant in the USH1G gene in a family with Usher syndrome [PDF]
BiomedicaGélvez N, López G, Tamayo ML.
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Intranasal application of a bifunctional pertactin-RTX fusion antigen elicits protection of mouse airway mucosa against <i>Bordetella pertussis</i> colonization. [PDF]
mSphereEspinosa-Vinals C +6 more
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[Autosomal recessive limb-girdle muscular dystrophy-10. Case report]. [PDF]
Rev Med Inst Mex Seguro SocPérez-Arzola AA +8 more
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Uso de inteligencia artificial en la predisposición genética a enfermedad crítica por COVID-19: evaluación comparativa de modelos de aprendizaje automático. [PDF]
Adv Lab MedMartin Perez S +9 more
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