Molecular genetics of the neuronal ceroid lipofuscinoses

Epilepsia

Volumn 40, Issue SUPPL. 3, 1999, Pages 29-32

  Mole, Sara ^a   Gardiner, Mark ^a  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

Batten disease; Genetics; Inherited disease; Neurogenetics; Neurology

Indexed keywords

ARGININE; COMPLEMENTARY DNA; GENE PRODUCT; MEMBRANE PROTEIN; PALMITOYL PROTEIN THIOESTERASE; PEPTIDASE; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATASE; RECEPTOR; RNA; TRYPTOPHAN;

CHROMOSOME; CLINICAL FEATURE; CONFERENCE PAPER; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; HUMAN; MOLECULAR GENETICS; NEURONAL CEROID LIPOFUSCINOSIS; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGE FACTORS; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; HUMANS; INCIDENCE; LINKAGE (GENETICS); MOLECULAR BIOLOGY; MUTATION; NEURONAL CEROID-LIPOFUSCINOSES;

EID: 0032793574     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1528-1157.1999.tb00896.x     Document Type: Conference Paper

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