This is a preview of subscription content, log in via an institution to check access.
References
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, J.A., Conneally, P.M., Fardeau, M., Cohen, D., Jackson, C.E., Beckmann, J.S. (1995). Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1 cM 15q15.1–q15.3 interval. Am. J. Hum. Genet. 56, 1417–1430.
Chiannilkulchai, N., Pasturaud, P., Richard, I., Auffray, C., Beckmann, J.S. (1995). A primary expression map of chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene. Hum. Mol. Genet 4, 717–726.
Chumakov, I.M., LeGall, I., Billault, A., Ougeu, P., Soularue, P., Guillou, S. Rigault, P., Bui, H., De Tand, M.-F., Barillot, E., Abderrahim, H., Cherif, D., Berger, R., Le Paslier, D., Cohen D. (1992). Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library. Nature Genet 1, 222–225.
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, J.S. (1994). Mapping of a chromosome 15 region involved in limb-girdle muscular dystrophy. Hum. Mol Genet. 3, 285–293.
Pereira de Souza, A., Allamand, V., Richard, I., Brenguier, L., Chumakov, I., Cohen, D., Beckmann J.S. (1994). Targeted development of microsatellite markers from inter-Alu amplification of YAC clones. Genomics 19, 391–393.
Richard, I., Broux, O., Chiannikulchai, N., Fougerousse, F., Allamand, V., Bourg, N., Brenguier, L., Devaud, C., Pasturaud, P., Roudaut, C., Lorenzo, F., Sebastiani-Kabatchis, C., Schultz, R.A., Polymeropoulos, M.H., Gyapay, G., Auffray, C. Beckmann, J.S., (1994) Regional localization of human chromosome 15 loci. Genomics 23, 619–627.
Richard, I., Broux, O., Allamand, V., Fougerousse, F., Chiannilkulchai, N., Bourg, N., Brenguier, L., Devaud, C., Pasturaud, P. Roudaut, C., Hillaire, D., Passos-Bueno, M.-R., Zatz, M., Tishfield, J.A., Fardeau, M., Jackson, C.E., Cohen, D., Beckmann, J.S., (1995). Mutations in the proteolytic enzyme, calpain 3, cause limb-girdle muscular dystrophy type 2A. Cell 81, 27–40.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Richard, I., Roudaut, C., Fougerousse, F. et al. An STS map of the limb girdle muscular dystrophy type 2A region. Mammalian Genome 6, 754–756 (1995). https://doi.org/10.1007/BF00354303
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00354303