TY  - JOUR 
AU  - Martínez-Rubio, D.
AU  - Hinarejos, I.
AU  - Argente-Escrig, H.
AU  - Marco-Marín, C.
AU  - Lozano, M.A.
AU  - Gorría-Redondo, N.
AU  - Lupo, V.
AU  - Martí-Carrera, I.
AU  - Miranda, C.
AU  - Vázquez López, Esther
AU  - García-Pérez, A.
AU  - Marco-Hernández, A.V.
AU  - Tomás-Vila, M.
AU  - Aguilera-Albesa, S.
AU  - Espinós, C.
PY  - 2023
SN  - 1422-0067
UR  - http://hdl.handle.net/20.500.11940/21529
AB  - Cerebellar atrophy (CA) is a frequent neuroimaging finding in paediatric neurology, usually associated with cerebellar ataxia. The list of genes involved in hereditary forms of CA is continuously growing and reveals its genetic complexity. We...
LA  - eng
KW  - Child
KW  - Humans
KW  - Genetic Heterogeneity
KW  - Mutation
KW  - Cerebellar Ataxia
KW  - Cerebellar Diseases
KW  - Ataxia
KW  - Phenotype
KW  - Spastic Paraplegia, Hereditary
KW  - Paraplegia
KW  - Neurodegenerative Diseases
KW  - Pedigree
KW  - Atrophy
KW  - Microtubule-Associated Proteins
KW  - Membrane Proteins
TI  - Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy
DO  - 10.3390/ijms242216400
T2  - International Journal of Molecular Sciences
KW  - AS Lugo
KW  - CHULA
VL  - 24
ER  -