Identification and Characterization of 15 Novel GALC Gene Mutations Causing Krabbe Disease

The characterization of the underlying GALC gene lesions was performed in 30 unrelated patients affected by Krabbe disease, an autosomal recessive leukodystrophy caused by the deficiency of lysosomal enzyme galactocerebrosidase. The GALC mutational spectrum comprised 33 distinct mutant (including 15...

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Detalles Bibliográficos
Autores principales: Tappino, Barbara, Biancheri, Roberta, Mort, Matthew, Regis, Stefano, Corsolini, Fabio, Rossi, Andrea, Stroppiano, Marina, Lualdi, Susanna, Fiumara, Agata, Bembi, Bruno, Di Rocco, Maja, Cooper, David N, Filocamo, Mirella
Formato: Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2010
Materias:
Mutation in Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052420/
https://www.ncbi.nlm.nih.gov/pubmed/20886637
http://dx.doi.org/10.1002/humu.21367

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052420/
https://www.ncbi.nlm.nih.gov/pubmed/20886637
http://dx.doi.org/10.1002/humu.21367

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