sábado, 24 de agosto de 2019

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page



New Articles For BioMed Central:

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases

RESEARCH

Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia

Giorgia Olivieri, Stefano Pro, Daria Diodato, Matteo Di Capua, Daniela Longo, Diego Martinelli, Enrico Bertini and Carlo Dionisi-Vici
Orphanet Journal of Rare Diseases 2019, 14:208 | Published on: 23 August 2019

Follow BMC on:Twitter IconFacebook IconYouTube IconLinkedIn Icon

For further information or enquiries please use our contact page details.
BMC respects your privacy and does not disclose, sell or rent your personal information to any non-affliated third parties with your consent. Privacy policy.
BioMed Central Ltd
The Campus, 4 Crinan Street,
London, N1 9XW,
United Kingdom
Springer Nature logo
© 2019 BioMed Central Limited unless otherwise stated. Part of Springer Nature.

No hay comentarios:

Publicar un comentario