A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia

Παρόμοια τεκμήρια

• Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia
  ανά: Paznekas, William A., κ.ά.
  Έκδοση: (2003)
• Two novel GJA1 variants in oculodentodigital dysplasia
  ανά: Pace, Nikolai P., κ.ά.
  Έκδοση: (2019)
• Novel Mutations in GJA1 Cause Oculodentodigital Syndrome
  ανά: Fenwick, A., κ.ά.
  Έκδοση: (2008)
• Dominant de novo mutations in GJA1 cause erythrokeratodermia variabilis et progressiva, without features of oculodentodigital dysplasia
  ανά: Boyden, Lynn M., κ.ά.
  Έκδοση: (2014)
• Arrhythmias in dilated cardiomyopathy.
  ανά: Neri, R., κ.ά.
  Έκδοση: (1986)