Batten disease (Spielmeyer‐Sjogren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16

Clinical Genetics

Volumn 36, Issue 4, 1989, Pages 217-218

  Eiberg, H ^a   Gardiner, R M ^b   Mohr, J ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b JOHN RADCLIFFE HOSPITAL   (United Kingdom)

Author keywords

Batten disease; chromosome 16; haptoglobin; linkage

Indexed keywords

HAPTOGLOBIN;

CHROMOSOME 16Q; CLINICAL ARTICLE; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; HEREDITY; HUMAN; HUMAN CELL; NEURONAL CEROID LIPOFUSCINOSIS; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 16; FEMALE; HAPTOGLOBINS; HUMAN; LINKAGE (GENETICS); LOD SCORE; MALE; NEURONAL CEROID-LIPOFUSCINOSIS; SUPPORT, NON-U.S. GOV'T;

EID: 0024450299     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1989.tb03193.x     Document Type: Article

References (4)

1. Linkage between serum cholin‐esterase 2 (CHE2) and γ‐crystallin gene cluster (CRYG): assignment to chromosome 2
2. A computer program for linkage analysis in human pedigrees
3. Die juvenile amaurotische Idiotic. Klinische und erblichkeitsmedizinische Untersuchungen