Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patients.

Những quyển sách tương tự

• Niemann-Pick disease: a frequent missense mutation in the acid sphingomyelinase gene of Ashkenazi Jewish type A and B patients.
  Bằng: Levran, O, et al.
  Được phát hành: (1991)
• The Demographics and Distribution of Type B Niemann-Pick Disease: Novel Mutations Lead to New Genotype/Phenotype Correlations
  Bằng: Simonaro, Calogera M., et al.
  Được phát hành: (2002)
• Types A and B Niemann-Pick Disease
  Bằng: Schuchman, Edward H., et al.
  Được phát hành: (2016)
• Enhanced Delivery and Effects of Acid Sphingomyelinase by ICAM-1-Targeted Nanocarriers in Type B Niemann-Pick Disease Mice
  Bằng: Garnacho, Carmen, et al.
  Được phát hành: (2017)
• Brain pathology in Niemann Pick disease type A: Insights from the acid sphingomyelinase knockout mice
  Bằng: Ledesma, Maria Dolores, et al.
  Được phát hành: (2011)