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References
Brown, C.J., Ballabio, A., Rupert, J.L., Lafreniere, R.G., Grompe, M., Tonlorenzi, R., and Willard, H.F. (1991). A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome. Nature 349, 38–44.
Brown, G.K., Haan, E.A., Kirby, D.M., Scholem, R.D., Wraith, J.E., Rogers, J.G., and Danks, D.M. (1988). “Cerebral” lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis. Eur. J. Pediatr. 147, 10–14.
Brown, R.M., Dahl, H.-H.M., and Brown, G.K. (1989). X Chromosome localization of the functional gene for the E1α subunit of the human pyruvate dehydrogenase complex. Genomics 4, 174–181.
Brown, R.M., Dahl, H.-H.M., and Brown, G.K. (1990). Pyruvate dehydrogenase E1α subunit genes in the mouse: mapping and comparison with human homologs. Som. Cell. Mol. Genet. 16, 487–492.
Brown, S.D.M., Avner, P., and Herman, G.E. (1992). Mouse X Chromosome. Mammalian Genome 3 (Suppl), S274-S278.
Dahl, H.-H.M., Hunt, S.M., Hutchison, W.M., and Brown, G.K. (1987). The human pyruvate dehydrogenase complex: isolation of cDNA clones for the E1α subunit, sequence analysis and characterisation of the mRNA. J. Biol. Chem. 262, 7398–7403.
Dahl, H.-H.M., Brown, R.M., Hutchison, W.M., Maragos, C., and Brown, G. (1990). A testis-specific form of the human pyruvate dehydrogenase E1α subunit is coded for by an intronless gene on chromosome 4. Genomics 8, 225–232.
Dautigny, A., Mattei, M.-G., Morello, D., Alliel, P.M., Pham-Dinh, D., Amar, L., Arnaud, D., Guénet, J.-L., Jollès, P., and Avner P. (1986). Structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice. Nature 321, 867–869.
Davies, K.E., Mandel, J.-L., Monaco, A.P., Nussbaum, R.L., and Willard, H.F. (1991). Report of committee on the genetic constitution of the X chromosome. Cytogenet. Cell Genet. 58, 853–966.
Evans, E.P. (1989). Standard normal chromosomes. In Genetic Variants and Strains of the Laboratory Mouse, M.F. Lyon, and A.G. Searle, eds. (Oxford: Oxford University Press), pp. 576–578.
Laval, S.H., Chen, Z.-Y., and Boyd, Y. (1991). The properdin structural locus (Pfc) lies close to the locus for tissue inhibitor of metalloproteinaes (Timp) on the mouse X chromosome. Genomics 10, 1030–1034.
Laval, S.H., Blair, H.J., Hirst, M.C., Davies, K.E., and Boyd, Y. (1992). Mapping of Fmr-1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome. Genomics 12, 818–821.
Maragos, C., Hutchison, W.N., Hayasaka, K., Brown, G.K., and Dahl, H.-H.M. (1989). Structural organisation of the gene for the E1α subunit of the human pyruvate dehydrogenase complex. J. Biol. Chem. 264, 12294–12298.
Milner, R.J., Lai, C., Nave, K.-A., Lenoir, D., Ogata, J., and Sutcliffe, J.G. (1985). Nucleotide sequences of two mRNAs for rat brain myelin proteolipid protein. Cell 42, 931–939.
Snead, M.L., Lau, E.C., Zeichner-David, M., Fincham, A.G., Woo, S.L.C., and Slarkin, H.C. (1985). DNA sequence for cloned cDNA for murine amelogenin reveals the amino acid sequence for enamel-specific protein. Biochem. Biophys. Res. Commun. 129, 812–818.
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Blair, H.J., Reed, V., Laval, S.H. et al. The locus for pyruvate dehydrogenase E1 α subunit (Pdha1) lies between Plp and Amg on the mouse X Chromosome. Mammalian Genome 4, 230–233 (1993). https://doi.org/10.1007/BF00417569
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DOI: https://doi.org/10.1007/BF00417569