Parliamentary Papers, Band 21 |
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Seite 67
Garrod suggested that in such conditions all the bio- chemical and clinical features could ultimately be explained in terms of a block at some point in intermediary metabolism , due to the congenital deficiency of a specific enzyme .
Garrod suggested that in such conditions all the bio- chemical and clinical features could ultimately be explained in terms of a block at some point in intermediary metabolism , due to the congenital deficiency of a specific enzyme .
Seite 71
For example , one type has been shown to be due to a deficiency of the enzyme dehalogenase , normally concerned with the deiodination of monoiodotyrosine and diiodotyrosine , and another type to a failure in the conversion of inorganic ...
For example , one type has been shown to be due to a deficiency of the enzyme dehalogenase , normally concerned with the deiodination of monoiodotyrosine and diiodotyrosine , and another type to a failure in the conversion of inorganic ...
Seite 72
These findings suggest that such heterozygotes have a partial deficiency of the enzyme that is almost completely absent in the affected homozygotes . In heterozygotes for the galactosaemia gene this partial deficiency of the enzyme has ...
These findings suggest that such heterozygotes have a partial deficiency of the enzyme that is almost completely absent in the affected homozygotes . In heterozygotes for the galactosaemia gene this partial deficiency of the enzyme has ...
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