2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: An X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease

1. García-Villoria, J.
2. Ofman, R.
3. Sala, P.R.
4. Merinero, B.
5. Ramos, J.
6. García-Silva, M.T.
7. Beseler, B.
8. Dalmau, J.
9. Wanders, R.J.A.
10. Ugarte, M.
11. Ribes, A.

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DOI: 10.1203/01.PDR.0000176916.94328.CD GOOGLE SCHOLAR lock_openOpen access editor

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