Impaired fertility and motor function in a zebrafish model for classic galactosemia

Classic galactosemia is a genetic disorder of galactose metabolism, caused by severe deficiency of galactose-1-phosphate uridylyltransferase (GALT) enzyme activity due to mutations of the GALT gene. Its pathogenesis is still not fully elucidated, and a therapy that prevents chronic impairments is la...

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Detalles Bibliográficos
Autores principales: Vanoevelen, Jo M., van Erven, Britt, Bierau, Jörgen, Huang, Xiaoping, Berry, Gerard T., Vos, Rein, Coelho, Ana I., Rubio-Gozalbo, M. Estela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786655/
https://www.ncbi.nlm.nih.gov/pubmed/28913702
http://dx.doi.org/10.1007/s10545-017-0071-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786655/
https://www.ncbi.nlm.nih.gov/pubmed/28913702
http://dx.doi.org/10.1007/s10545-017-0071-1

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