Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping

American Journal of Human Genetics

Volumn 64, Issue 1, 1999, Pages 126-135

  Cormand, Bru ^a,b   Avela, Kristiina ^a,b   Pihko, Helena ^c   Santavuori, Pirkko ^c   Talim, Beril ^d   Topaloglu, Haluk ^d   De La Chapelle, Albert ^a,b   Lehesjoki, Anna Elina ^a,b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b FOLKHÄLSAN INSTITUTE OF GENETICS   (Finland)

^c HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^d HACETTEPE UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN DISEASE; CHROMOSOME 1P; CONTROLLED STUDY; EYE DISEASE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENOME; GENOTYPE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; HUMAN CELL; MUSCLE DISEASE; PRIORITY JOURNAL;

EID: 0033360965     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302206     Document Type: Article

References (4)

1. Avela K, Lipsanen-Nyman M, Perheentupa J, Wallgren-Petterson C, Marchand S, Fauré S, Sistonen P, et al (1997) Assignment of the mulibrey nanism gene to 17q by linkage analysis and allelic association. Am J Hum Genet 60:896-902
2. Bönnemann CG, Modi R, Noguchi S, Mizuno Y, Yoshida M, Gussoni E, McNally EM, et al (1995) β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Nat Genet 11:266-273
3. Voit T (1998) Congenital muscular dystrophies: 1997 update. Brain Dev 20:65-74
4. Weeks DE, Ott J, Lathrop GM (1990) SLINK: a general simulation program for linkage analysis. Am J Hum Genet 47 (suppl):A204