Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency. (Q46035650)
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scientific article published on 27 April 2009
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency. |
scientific article published on 27 April 2009 |
Statements
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Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency. (English)
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B Shanti
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M Silink
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K Bhattacharya
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N J Howard
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K Carpenter
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M Fietz
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P Clayton
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27 April 2009
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32 Suppl 1
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S241-51
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