tyrosine and Encephalomyopathies, Mitochondrial

tyrosine has been researched along with Encephalomyopathies, Mitochondrial in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Dimauro, S; Hirano, M; Naini, A; Navas, P; Quinzii, C; Salviati, L; Trevisson, E	1

Other Studies

1 other study(ies) available for tyrosine and Encephalomyopathies, Mitochondrial

Article	Year
A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency. American journal of human genetics, 2006, Volume: 78, Issue:2 Topics: Alkyl and Aryl Transferases; Amino Acid Sequence; Amino Acid Substitution; Child, Preschool; Coenzymes; Cysteine; Female; Fibroblasts; Humans; Infant; Male; Mitochondrial Encephalomyopathies; Molecular Sequence Data; Mutation; Mutation, Missense; Tyrosine; Ubiquinone	2006

Article

Year

A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency.

American journal of human genetics, 2006, Volume: 78, Issue:2

Topics: Alkyl and Aryl Transferases; Amino Acid Sequence; Amino Acid Substitution; Child, Preschool; Coenzymes; Cysteine; Female; Fibroblasts; Humans; Infant; Male; Mitochondrial Encephalomyopathies; Molecular Sequence Data; Mutation; Mutation, Missense; Tyrosine; Ubiquinone

2006