From locus to cellular disturbances: positional cloning of the infantile neuronal ceroid lipofuscinosis gene.

Hellsten, E; Vesa, J; Jalanko, A; Peltonen, L

Hellsten, E; Vesa, J; Jalanko, A; Peltonen, L.

Affiliation

Hellsten E; National Public Health Institute, Department of Human Molecular Genetics, Helsinki, Finland.

Neuropediatrics ; 28(1): 9-11, 1997 Feb.

Article in En | MEDLINE | ID: mdl-9151310

Subject(s)

Chromosome Mapping; Cloning, Molecular; Neuronal Ceroid-Lipofuscinoses/genetics; Adolescent; Child; Child, Preschool; Chromosome Aberrations/genetics; Chromosome Disorders; Chromosomes, Human, Pair 1; DNA Mutational Analysis; Finland; Genes, Recessive/genetics; Humans; Infant; Neuronal Ceroid-Lipofuscinoses/classification; Neuronal Ceroid-Lipofuscinoses/diagnosis; Palmitoyl-CoA Hydrolase/genetics

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Mapping / Cloning, Molecular / Neuronal Ceroid-Lipofuscinoses Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Child / Child, preschool / Humans / Infant Country/Region as subject: Europa Language: En Journal: Neuropediatrics Year: 1997 Document type: Article Affiliation country: Finland Country of publication: Germany

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