https://pubmed.ncbi.nlm.nih.gov/20820830/
A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis
A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis
https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2022.942667/full
Frontiers | Cardiac magnetic resonance findings in neuronal ceroid lipofuscinosis: A case report
Cardiac magnetic resonance imaging (MRI) is an essential tool for the study of hypertrophic cardiomyopathies (HCM) and for differentiating HCM from condition...
magnetic resonance
https://www.wikidata.org/wiki/Q34350902
Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32:...
https://www.semanticscholar.org/topic/Ceroid-Lipofuscinosis%2C-Neuronal%2C-Parry-Type/12279462
Ceroid Lipofuscinosis, Neuronal, Parry Type | Semantic Scholar
neuronalparrytypesemanticscholar