Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome.

Benzer Materyaller

• Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus.
  Yazar:: Myers, J C, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders.
  Yazar:: Mueller, O T, ve diğerleri
  Baskı/Yayın Bilgisi: (1986)
• Mannosidosis: assignment of the lysosomal alpha-mannosidase B gene to chromosome 19 in man.
  Yazar:: Champion, M J, ve diğerleri
  Baskı/Yayın Bilgisi: (1977)
• Comparative distribution of the alpha 1(IV), alpha 5(IV), and alpha 6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patients.
  Yazar:: Peissel, B, ve diğerleri
  Baskı/Yayın Bilgisi: (1995)
• Molecular and functional defects in kidneys of mice lacking collagen alpha 3(IV): implications for Alport syndrome
  Baskı/Yayın Bilgisi: (1996)