– MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death
– Genome-wide associations for birth weight and correlations with adult disease
– Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality
– Genome-wide analysis identifies 12 loci influencing human reproductive behavior
– Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
Mutaciones y polimorfismos de riesgo para cardiopatías, conducta reproductiva, fragilidad cutánea y otras
Filed under Cardiopatías, Defectos congénitos, Diagnóstico, Polimorfismos by on . 
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