Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones.

Những quyển sách tương tự

• An endoplasmic reticulum storage disease causing congenital goiter with hypothyroidism
  Được phát hành: (1996)
• A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: A model of human endoplasmic reticulum storage diseases
  Bằng: Kim, Paul S., et al.
  Được phát hành: (1998)
• A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism.
  Bằng: Ieiri, T, et al.
  Được phát hành: (1991)
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  Được phát hành: (2010)
• A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant
  Bằng: Eve Stern, et al.
  Được phát hành: (2022-06-01)