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Results 1 - 9 of 9 for Homozygote
  1. ... P. Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human ...
  2. ... copies of the GRN gene in each cell (homozygotes) do not produce any functional progranulin protein. These ...
  3. ... and reduced life span of oculopharyngeal muscular dystrophy homozygotes. Neurology. 2009 Aug 25;73(8):596-601. ...
  4. ... copies of the MSTN gene in each cell (homozygotes) have significantly increased muscle mass and strength. People ...
  5. ... multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279W. J Med Genet. 2003 ...
  6. ... HY. Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase Deficiency. ...
  7. ... P. Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human ...
  8. ... HY. Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase Deficiency. ...
  9. How Is Wilson Disease Inherited? (Wilson Disease Association)  
    Wilson Disease/Genetics ... Wilson Disease ... Wilson Disease Association