ಶೋಧನೆಯ ಫಲಿತಾಂಶಗಳು

neuronal ceroid lipofuscinosis: Human disease

juvenile neuronal ceroid lipofuscinosis: extremely rare and fatal autosomal recessive neurodegenerative disorder in humans

Infantile neuronal ceroid lipofuscinosis: Neuronal ceroid lipofuscinosis

Jansky–Bielschowsky disease: autosomal recessive genetic disorder

CLN8: protein-coding gene in the species Homo sapiens

Kufor-Rakeb syndrome: Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment