Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation. (Q50335655)
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scientific article published in November 2000
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation. |
scientific article published in November 2000 |
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Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation. (English)
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Wang Y
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Taroni F
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1 November 2000
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16
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5
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401-407
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