Eduardo P. Mattos
Porto Alegre, RS, Brazil
Last Updated: 09/26/2026
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Found 10 publications
Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.
Journal: Cerebellum (London, England)
Published: January 16, 2020
Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.
Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.
Journal: Cerebellum (London, England)
Published: January 05, 2020
Correction to: Selective Forces Related to Spinocerebellar Ataxia Type 2.
Journal: Cerebellum (London, England)
Published: November 20, 2018
Selective Forces Related to Spinocerebellar Ataxia Type 2.
Journal: Cerebellum (London, England)
Published: September 17, 2018
Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions.
Journal: Clinical genetics
Published: November 07, 2015
Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence.
Journal: Neurogenetics
Published: October 19, 2015
Clinical and Molecular Characterization of Osteogenesis Imperfecta Type V.
Journal: Molecular syndromology
Published: August 04, 2015
Infantile spinocerebellar ataxia type 7: Case report and a review of the literature.
Journal: Journal of the neurological sciences
Published: February 26, 2015
Identification of a premature stop codon mutation in the PHGDH gene in severe Neu-Laxova syndrome-evidence for phenotypic variability.
Journal: American journal of medical genetics. Part A
Published: September 30, 2014
Clinical and molecular characterization of a Brazilian cohort of campomelic dysplasia patients, and identification of seven new SOX9 mutations.
Journal: Genetics and molecular biology
Published: May 08, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026