학술논문
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosis
Document Type
Article
Author
Aiello, C.; Terracciano, A.; Cannelli, N.; Claps, D.; Bianchi, M.; Longo, D.; Tessa, A.; Boldrini, R.; Bertini, E.S.; Carrozzo, R.; Santorelli, F.M.; Simonati, A.; Tavoni, A.; Discepoli, G.; Crow, Y.J.; Kitzmuller, C.; Mole, S.E.; Franzoni, E.; Veneselli, E.; Filocamo, M.; Biancheri, R.; Williams, R.E.
Source
In: Human Mutation . (Human Mutation, March 2009, 30(3):E530-E540)
Subject
Language
English
ISSN
10597794