3
results
for author:"Grebe T.A."
in Literature Citations
| The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle. Brautbar A., Wang J., Abdenur J.E., Chang R.C., Thomas J.A., Grebe T.A., Lim C., Weng S.W., Graham B.H., Wong L.J. Mol. Genet. Metab. 94:485-490(2008) · Mapped (5) |
| Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. del Gaudio D., Fang P., Scaglia F., Ward P.A., Craigen W.J., Glaze D.G., Neul J.L., Patel A., Lee J.A., Irons M. et al. Genet. Med. 8:784-792(2006) · Mapped (5) |
| Human chromosome 7: DNA sequence and biology. Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R. et al. Science 300:767-772(2003) · UniProtKB (658) |
