MIREN AMETSA
SÁENZ PEÑA
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Instituto de Biomedicina de Valencia
Valencia, EspañaPublikationen in Zusammenarbeit mit Forschern von Instituto de Biomedicina de Valencia (5)
2011
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Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?
Muscle and Nerve, Vol. 44, Núm. 5, pp. 710-714
2008
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Mutations in Progranulin Gene: Clinical, Pathological, and Ribonucleic Acid Expression Findings
Biological Psychiatry, Vol. 63, Núm. 10, pp. 946-952
2006
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Parkinson's disease due to the R1441G mutation in Dardarin: A founder effect in the Basques
Movement Disorders, Vol. 21, Núm. 11, pp. 1954-1959
2005
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Familial Parkinson's disease: Clinical and genetic analysis of four Basque families
Annals of Neurology, Vol. 57, Núm. 3, pp. 365-372
2002
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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
Human Molecular Genetics, Vol. 11, Núm. 9, pp. 1119-1128