Homozygous E387K (1159G>A) mutation of the CYP1B1 gene in a Roma boy affected with primary congenital glaucoma. Case report

Gábor Vogt, Ľudevit/Lajos Kádasi, Endre Czeizel
  • Orvosi Hetilap, August 2014, Akademiai Kiado
  • DOI: 10.1556/oh.2014.29960

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http://dx.doi.org/10.1556/oh.2014.29960