Work

SPG11 sequencing in worldwide populations of familial and sporadic spastic paraplegia patients reveals frequent mutations and the common association of parkinsonian features

Year: 2013

Type: article

Source: UCL Discovery (University College London)

Authors: Eleanna Kara, Lucía Schottlaender, Andrés Berardo, Ricardo Reisin, Jason Hehir, David Hughes, Raju Paudel, Joshua Hersheson, Liu Yt, Elisavet Preza, Patrick A. Lewis, Alba Martín-Yebra, Prasad Korlipara, Kailash P. Bhatia, A. Lees, Thomas Foltynie, Nicholas Wood, John Hardy, Henry Houlden

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W362033349

FWCI:

Cites:

Cited by:

Related to: 10