Genotype-phenotype analyses of classic neuronal ceroid lipofuscinosis (NCLs): genetic predictions from clinical and pathological findings

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

Volumn 38, Issue 1, 2006, Pages 41-48

  Ju, Weina ^a   Wronska, Anetta ^b   Moroziewicz, Dorota N ^b   Zhong, Rocksheng ^b   Wisniewski, Natalia ^b   Jurkiewicz, Anna ^b   Fiory, Michael ^b   Wisniewski, Krystyna E ^b   Johnston, Lance ^b   Brown, W Ted ^b   Zhong, Nanbert ^b  

^a NEW YORK STATE INSTITUTE FOR BASIC RESEARCH IN DEVELOPMENTAL DISABILITIES   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AMINOPEPTIDASE; CHAPERONE; CLN3 PROTEIN, HUMAN; DIPEPTIDYL PEPTIDASE; MEMBRANE PROTEIN; PPT1 PROTEIN, HUMAN; SERINE PROTEINASE; TRIPEPTIDYL-PEPTIDASE 1;

CELL GRANULE; GENETIC ASSOCIATION STUDY; GENETICS; GENOTYPE; HUMAN; MUTATION; NEURONAL CEROID LIPOFUSCINOSIS; ONSET AGE; PATHOLOGY; PEDIGREE; PHENOTYPE;

AGE OF ONSET; AMINOPEPTIDASES; CYTOPLASMIC GRANULES; DIPEPTIDYL-PEPTIDASES AND TRIPEPTIDYL-PEPTIDASES; GENETIC ASSOCIATION STUDIES; GENOTYPE; HUMANS; MEMBRANE GLYCOPROTEINS; MEMBRANE PROTEINS; MOLECULAR CHAPERONES; MUTATION; NEURONAL CEROID-LIPOFUSCINOSES; PEDIGREE; PHENOTYPE; SERINE PROTEASES;

EID: 34250781863     PISSN: 1671167X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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