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Results 1 - 6 of 6 for Ceroid lipofuscinosis neuronal 8
  1. CLN8 disease 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov CEROID LIPOFUSCINOSIS, NEURONAL, 8; CLN8 CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT ...
    https://medlineplus.gov/genetics/condition/cln8-disease - Genetics
  2. CLN1 disease 
    ... and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses. Hum Mutat. 2012 Jan;33(1):42-63. ...
    https://medlineplus.gov/genetics/condition/cln1-disease - Genetics
  3. CLN10 disease 
    ... and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses. Hum Mutat. 2012 Jan;33(1):42-63. ...
    https://medlineplus.gov/genetics/condition/cln10-disease - Genetics
  4. CLN3 disease 
    ... PubMed Rakheja D, Narayan SB, Bennett MJ. Juvenile neuronal ceroid-lipofuscinosis (Batten disease): a brief review and update. Curr Mol Med. 2007 Sep;7(6):603-8. doi: 10.2174/156652407781695729. Citation on PubMed Schulz ...
    https://medlineplus.gov/genetics/condition/cln3-disease - Genetics
  5. CLN4 disease 
    ... of cases: study of the Parry family and 8 other families. PLoS One. ... for the neuronal ceroid lipofuscinoses. Neurology. 2012 Jul 10;79(2):183-91. ...
    https://medlineplus.gov/genetics/condition/cln4-disease - Genetics
  6. CLN11 disease 
    ... disease type is given the designation "CLN," meaning ceroid lipofuscinosis, neuronal, and then a number to indicate its subtype. ... progranulin protein develop GRN-related frontotemporal lobar degeneration. Ceroid lipofuscinosis, neuronal, 11 GRN-related neuronal ceroid-lipofuscinosis Genetic Testing ...
    https://medlineplus.gov/genetics/condition/cln11-disease - Genetics