Unique variants in the FLG gene and FERMT1 gene in a Chinese patient with ichthyosis and Kindler syndrome

Samankaltaisia teoksia

• Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
  Tekijä: Oh, Seung Joon, et al.
  Julkaistu: (2016)
• A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome
  Tekijä: GAO, Ying, et al.
  Julkaistu: (2015)
• A novel frameshift mutation in the FERMT1 gene in a Chinese patient with Kindler syndrome
  Tekijä: Meng, Li, et al.
  Julkaistu: (2020)
• Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report
  Tekijä: Wang, Xiong, et al.
  Julkaistu: (2018)
• Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients
  Tekijä: Kim, Eun Joo, et al.
  Julkaistu: (2011)