Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family
(Q73876289)
scientific article published on 01 May 2001
scientific article published on 01 May 2001
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Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family
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| description | scientific article published on 01 May 2001 |
External Links
| (P356) |
10.1006/MGME.2001.3162
|
| (P698) |
11350184
|