Limb girdle muscular dystrophy type 2A (CAPN3): Mapping using allelic association

Human Heredity

Volumn 48, Issue 6, 1998, Pages 333-337

  Lonjou, Christine ^a   Collins, Andrew ^a   Beckmann, Jacques ^b   Allamand, Valérie ^c   Morton, Newton ^a  

^a UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^b CNRS   (France)

^c UNIVERSITY OF IOWA   (United States)

Author keywords

Gene mapping; Linkage disequilibrium; Malecot model

Indexed keywords

NEUTRAL PROTEINASE;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; HAPLOTYPE; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY;

ALLELES; CALPAIN; GENES, RECESSIVE; GENETIC MARKERS; HUMANS; ISOENZYMES; LINKAGE DISEQUILIBRIUM; MODELS, GENETIC; MUSCLE PROTEINS; MUSCULAR DYSTROPHIES; PEPTIDE FRAGMENTS;

EID: 0031792221     PISSN: 00015652     EISSN: None     Source Type: Journal    
DOI: 10.1159/000022825     Document Type: Article

References (11)

1. Fougerousse F, Broux O, Richard I, Allamand V, Pereira de Souza A, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, Chiannilkulchai N, Hillaire D, Bui H, Chumakov I, Weissenbach J, Cherif D, Cohen D, Beckmann JS: Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy. Hum Mol Genet 1994;3:285-293.
2. Allamand V, Broux O, Richard I, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, Devaud C, Pasturaud P, Pereira de Souza A, Roudaut C, Tischfield JA, Conneally PM, Fardeau M, Cohen D, Jackson CE, Beckmann JS: Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 inteval. Am J Hum Genet 1995;56:1417-1430.
3. Richard I, Broux O, Allamand V, Fourgerousse F, Chiannilkulchai N, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, Hillaire D, Passos-Bueno MR, Zatz M, Tischfield JA, Fardeau M, Jackson CE, Cohen D, Beckmann J: Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A. Cell 1995;81:27-40.
4. Allamand V, Beckmann JS: Mapping using linkage disequilibrium estimates: A comparative study. Hum Hered 1997;47:237-240.
5. Collins A, Morton NE: Mapping a disease locus by allelic association. Proc Natl Acad Sci USA 1998;95: 1741-1745.
6. Collins A, Ajioka RS, Jorde LB, Lonjou C, Morton NE: Hemochromatosis (HFE): Mapping by allelic association under recombinational heterogeneity. Submitted.
7. Morton NE, Lew R, Hussels IE, Little GF: Pingelap and Mokil atolls: Historical genetics. Am J Hum Genet 1972;24:277-289.
8. Devlin B, Risch N: A comparison of linkage disequilibrium measures for fine-scale mapping. Genomics 1995; 29:311-322.
9. Lehesjoki A-E, Koskiniemi M, Norio R, Tirrito S, Sistonen P, Lander E, de la Chapelle A: Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: Linkage disequilibrium allows high resolution mapping. Hum Mol Genet 1993;2:1229-1234.
10. Terwilliger JD: A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. Am J Hum Genet 1995;56: 777-787.
11. Lonjou C, Collins A, Morton NE: Huntington disease (HD): A trial of mapping polyphyletic alleles by association. Submitted.