Novel FH mutation associated with multiple uterine leiomyomas in Chinese siblings

Ítems similars

• MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas
  per: Kämpjärvi, Kati, et al.
  Publicat: (2016)
• Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas
  per: Barker, K T, et al.
  Publicat: (2002)
• Comparative Analysis of AKT and the related biomarkers in uterine leiomyomas with MED12, HMGA2 and FH mutations
  per: Xie, Jia, et al.
  Publicat: (2018)
• Novel Fumarate Hydratase Mutation in Siblings With Early Onset Uterine Leiomyomas and Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome
  per: Gunnala, Vinay, et al.
  Publicat: (2018)
• Multiple Uterine Leiomyomas in Multiple Endocrine Neoplasia Type 1 with a Novel MEN1 Gene Mutation
  per: Misgar, Raiz Ahmad, et al.
  Publicat: (2020)