Erratum to: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases

Samankaltaisia teoksia

• Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases
  Tekijä: Komlósi, Katalin, et al.
  Julkaistu: (2012)
• Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome
  Tekijä: Komlósi, Katalin, et al.
  Julkaistu: (2015)
• Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype
  Tekijä: Hadzsiev, Kinga, et al.
  Julkaistu: (2016)
• Role of carnitine and its derivatives in the development and management of type 2 diabetes
  Tekijä: Bene, Judit, et al.
  Julkaistu: (2018)
• Deletion of 4q28.3-31.23 in the background of multiple malformations with pulmonary hypertension
  Tekijä: Duga, Balazs, et al.
  Julkaistu: (2014)