A Novel PCCA Mutation in a Patient With Late-Onset Propionic Acidemia Identified by Genetic Diagnosis Panel

Những quyển sách tương tự

• A Novel PCCA Mutation in a Patient With Late-Onset Propionic Acidemia Identified by Genetic Diagnosis Panel
  Bằng: Yanyun Wang, et al.
  Được phát hành: (2018-08-01)
• Propionic acidemia identified in twin siblings conceived by in vitro fertilization (IVF) with parents who were unknown carriers of a PCCA mutation
  Bằng: Tian, Ye, et al.
  Được phát hành: (2020)
• A novel delins (c.773_819+47delinsAA) mutation of the PCCA gene associated with neonatal-onset propionic acidemia: a case report
  Bằng: Wang, Hai-rong, et al.
  Được phát hành: (2020)
• Case reports: three novel variants in PCCA and PCCB genes in Chinese patients with propionic acidemia
  Bằng: Yang, Qi, et al.
  Được phát hành: (2020)
• Biochemical and genetic approaches to the prenatal diagnosis of propionic acidemia in 78 pregnancies
  Bằng: Dai, Mengyao, et al.
  Được phát hành: (2020)