Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality (Q28140684)
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scientific article (publication date: 2 August 1999)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality |
scientific article (publication date: 2 August 1999) |
Statements
Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality (English)
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2 August 1999
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261
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2
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484-7
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