Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family (Q73876289)
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scientific article published on 01 May 2001
Language | Label | Description | Also known as |
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English | Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family |
scientific article published on 01 May 2001 |
Statements
Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family (English)
Yang BZ
Mallory JM
Roe DS
Brivet M
Strobel GD
Jones KM
Ding JH