Deficits of facial emotion recognition and visual information processing in adult patients with classical galactosemia
Author:
Funder
Galaktosämie Schweiz Patient Organization
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics (clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13023-019-0999-3.pdf
Reference33 articles.
1. Bosch AM. Classical galactosaemia revisited. J Inherit Metab Dis. 2006;29(4):516–25.
2. Berry GT, Walter JH. Disorders of Galactose Metabolism. In: Saudubray JM, van den Berghe G, Walter JH. editors. Inborn Metab Dis. Berlin: Springer; 2012. p. 141–50.
3. Calderon FR, Phansalkar AR, Crockett DK, Miller M, Mao R. Mutation database for the galactose-1-phosphate uridyltransferase (GALT) gene. Hum Mutat. 2007;28(10):939–43.
4. Ficicioglu C, Thomas N, Yager C, Gallagher PR, Hussa C, Mattie A, et al. Duarte (DG) galactosemia: a pilot study of biochemical and neurodevelopmental assessment in children detected by newborn screening. Mol Genet Metab. 2008;95(4):206–12.
5. Schweitzer S, Shin Y, Jakobs C, Brodehl J. Long-term outcome in 134 patients with galactosaemia. Eur J Pediatr. 1993;152(1):36–43.
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