- Galactosemia Detected by Neonatal Screening Test
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Park IS, Cho HJ, Lee DH, Song JH
- KMID: 2335722
- J Korean Pediatr Soc.
- 2003 May;46(5):440-446.
PURPOSE: The genetic disturbance of galactosemia is expressed as a cellular deficiency of either galactose-1-phosphate uridyltransferase(GALT) or galactokinase(GALK) or UDP galactose 4-epimerase(GALE). To find-out the pattern of galactosemia in Korea,... -
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