檢索結果 - Largilliere, C

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
    Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation.

    Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation. 由 Largillière, C., Vianey-Saban, C., Fontaine, M., Bertrand, C., Kacet, N., Farriaux, J. P.

    出版 1995
    獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:
  2. 2
    Site specific screening for point mutations in ornithine transcarbamylase deficiency.

    Site specific screening for point mutations in ornithine transcarbamylase deficiency. 由 Feldmann, D, Rozet, J M, Pelet, A, Hentzen, D, Briand, P, Hubert, P, Largilliere, C, Rabier, D, Farriaux, J P, Munnich, A

    出版 1992
    獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:
  3. 3
    Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.

    Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness. 由 Manouvrier, S, Rötig, A, Hannebique, G, Gheerbrandt, J D, Royer-Legrain, G, Munnich, A, Parent, M, Grünfeld, J P, Largilliere, C, Lombes, A

    出版 1995
    獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:

檢索工具: