[Mental retardation and hereditary enzymopathy (review)].

Subjects

Subjects :

Ammonia
Carboxy-Lyases metabolism
Child
Child, Preschool
Galactosemias genetics
Growth Disorders
Hartnup Disease genetics
Hepatolenticular Degeneration genetics
Homocystinuria genetics
Humans
Hydro-Lyases metabolism
Infant, Newborn
Intestinal Absorption
Lipidoses genetics
Male
Maple Syrup Urine Disease genetics
Mucopolysaccharidoses genetics
Phenylalanine Hydroxylase metabolism
Phenylketonurias genetics
Renal Aminoacidurias genetics
Eye Diseases genetics
Intellectual Disability genetics
Kidney Diseases genetics
L-Serine Dehydratase metabolism
Ligases metabolism
Lyases metabolism
Metabolism, Inborn Errors genetics
Mixed Function Oxygenases metabolism
Nucleotidyltransferases metabolism

Details

Language :

Russian

ISSN :

0044-4588

Volume :

71

Issue :

10

Database :

MEDLINE

Journal :

Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952)

Publication Type :

Academic Journal

Accession number :

5003148