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Hereditary causes include genetic defects in the metabolism of amino acids, cholesterol, and fatty acids, such as propionyl-CoA carboxylase deficiency (aka propionic acidemia) and medium chain acyl-CoA dehydrogenase deficiency (36)

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After disintegration, the so-obtained cell extract (homogenate) was centrifuged (11000 g , 5 min, 4 C), and the liquid was transferred to new test tubes and were frozen and stored at 80 C for biochemical analyses

En el caso de menores de edad, Mount Sinai seala que es importante consultar a un especialista en nutricin o un profesional de la salud, ya que el consumo de suplementos sin ningn tipo de supervisin mdica supone un riesgo