Page last updated: 2024-09-05

beta-methylcrotonylglycine and Auditory Processing Disorder, Central

beta-methylcrotonylglycine has been researched along with Auditory Processing Disorder, Central 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
Baumgartner, MR; Biberoglu, G; Demir, E; Eminoglu, FT; Hasanoglu, A; Okur, I; Ozcelik, AA; Tumer, L	1

Other Studies

1 other study(ies) available for beta-methylcrotonylglycine and Auditory Processing Disorder, Central

Article	Year
3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family. Journal of child neurology, 2009, Volume: 24, Issue:4 Topics: Adult; Brain; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child, Preschool; DNA Mutational Analysis; Epilepsy; Fibroblasts; Gene Deletion; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glycine; Humans; Infant; Language Development Disorders; Male; Mutation; Phenotype; Valerates	2009

Article

Year

3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family.

Journal of child neurology, 2009, Volume: 24, Issue:4

Topics: Adult; Brain; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child, Preschool; DNA Mutational Analysis; Epilepsy; Fibroblasts; Gene Deletion; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glycine; Humans; Infant; Language Development Disorders; Male; Mutation; Phenotype; Valerates

2009