Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease

• Autorzy: Cannizzaro M. , Jarosova J. , De Paepe B.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2019
• Tom: 60
• Numer: 3-4
• Opis fizyczny: p.305-317,ref.

Twórcy

autor

Cannizzaro M.

• Department of Neurology and Neuromuscular Reference Center, Ghent University Hospital, Ghent, Belgium

autor

Jarosova J.

• Department of Neurology and Neuromuscular Reference Center, Ghent University Hospital, Ghent, Belgium

autor

De Paepe B.

• Department of Neurology and Neuromuscular Reference Center, Ghent University Hospital, Ghent, Belgium

Identyfikatory

DOI

10.1007/s13353-019-00502-1