Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In). (Q51780425)
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scientific article published on 11 March 2009
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In). |
scientific article published on 11 March 2009 |
Statements
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In). (English)
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P T Clayton
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S Grunewald
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11 March 2009
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32 Suppl 1
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S137-9
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