Re: Hypergonadotropic hypogonadism in a patient with inv ins (2;4)

Int J Androl. 2009 Aug;32(4):429. doi: 10.1111/j.1365-2605.2008.00934.x. Epub 2008 Dec 9.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Comment

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 19*
  • Chromosomes, Human, Pair 2*
  • Chromosomes, Human, Pair 4*
  • Genetic Predisposition to Disease
  • Humans
  • Hypogonadism / genetics*
  • Male
  • Myotonic Dystrophy / complications
  • Myotonic Dystrophy / genetics*
  • Myotonin-Protein Kinase
  • Protein Serine-Threonine Kinases / genetics*
  • Translocation, Genetic*
  • Trinucleotide Repeat Expansion

Substances

  • DMPK protein, human
  • Myotonin-Protein Kinase
  • Protein Serine-Threonine Kinases