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Causes of Carnitine palmitoyl transferase II deficiency, lethal neonatal form

Causes of Carnitine palmitoyl transferase II deficiency, lethal neonatal form

The lethal neonatal form of carnitine palmitoyl transferase II deficiency is caused by a mutation in the carnitine palmitoyltransferase 2 gene, CPT2.

Carnitine palmitoyl transferase II deficiency, lethal neonatal form: Related Medical Conditions

To research the causes of Carnitine palmitoyl transferase II deficiency, lethal neonatal form, consider researching the causes of these these diseases that may be similar, or associated with Carnitine palmitoyl transferase II deficiency, lethal neonatal form:

Carnitine palmitoyl transferase II deficiency, lethal neonatal form: Causes and Types

Causes of Broader Categories of Carnitine palmitoyl transferase II deficiency, lethal neonatal form: Review the causal information about the various more general categories of medical conditions:

Related information on causes of Carnitine palmitoyl transferase II deficiency, lethal neonatal form:

As with all medical conditions, there may be many causal factors. Further relevant information on causes of Carnitine palmitoyl transferase II deficiency, lethal neonatal form may be found in:

 

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