Lysosomal dysfunction in TMEM106B hypomyelinating leukodystrophy

Ítems similars

• A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy
  per: Simons, Cas, et al.
  Publicat: (2017)
• Functional Study of <i>TMEM163</i> Gene Variants Associated with Hypomyelination Leukodystrophy
  per: Huifang Yan, et al.
  Publicat: (2022-04-01)
• TMEM106B and myelination: rare leukodystrophy families reveal unexpected connections
  per: Zhou, Xiaolai, et al.
  Publicat: (2017)
• Concordance between whole‐exome sequencing and clinical Sanger sequencing: implications for patient care
  per: Hamilton, Alison, et al.
  Publicat: (2016)
• Hypomyelinating leukodystrophy-associated mutation of RARS leads it to the lysosome, inhibiting oligodendroglial morphological differentiation
  per: Matsumoto, Naoto, et al.
  Publicat: (2019)