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oa South African Medical Journal - Galactosaemia in three Rhodesian infants

 

Abstract

The clinically relevant types of genetic galactosaemia involve deficiency of galactose-1-phosphate uridyltransferase (EC 2.7.7.12) or galactokinase (EC 2.7.1.6).

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/content/m_samj/55/8/AJA20785135_19654
1979-02-01
2016-12-08
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