No abstract available
MeSH terms
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Cardiomyopathy, Hypertrophic / etiology*
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Chromosomes, Human, Pair 16
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Congenital Disorders of Glycosylation / blood
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Congenital Disorders of Glycosylation / complications*
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Congenital Disorders of Glycosylation / genetics
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Fatal Outcome
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Fetal Diseases / etiology*
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Humans
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Infant, Newborn
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Male
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Pericardial Effusion / etiology*
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Transferrin / analogs & derivatives
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Transferrin / metabolism
Substances
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Transferrin
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carbohydrate-deficient transferrin