Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23

Human Molecular Genetics

Volumn 6, Issue 4, 1997, Pages 591-595

  Sharp, J D ^a   Wheeler, R B ^a   Lake, B D ^b   Savukoski, M ^c   Jarvela I E ^c   Peltonen, L ^c   Gardiner, R M ^a   Williams, R E ^a  

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

^b GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^c NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 11P; CHROMOSOME 15Q; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; GENE MAPPING; GENETIC LINKAGE; HOMOZYGOSITY; HUMAN; MALE; NEURONAL CEROID LIPOFUSCINOSIS; ONSET AGE; PRIORITY JOURNAL;

CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 15; CONSANGUINITY; FEMALE; GENETIC MARKERS; GENETIC SCREENING; GENOTYPE; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; NEURONAL CEROID-LIPOFUSCINOSES; PEDIGREE; PHENOTYPE;

EID: 0030937327     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.4.591     Document Type: Article

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