Peters Plus Syndrome Is Caused by Mutations in B3GALTL, a Putative Glycosyltransferase

Ngā tūemi rite

• Peters Plus Syndrome Is Caused by Mutations in B3GALTL, a Putative Glycosyltransferase
  mā: Lesnik Oberstein, Saskia A. J., me ētahi atu.
  I whakaputaina: (2006)
• Mutation Analysis of B3GALTL in Peters Plus Syndrome
  mā: Reis, Linda M., me ētahi atu.
  I whakaputaina: (2008)
• Peters Plus Syndrome Is a New Congenital Disorder of Glycosylation and Involves Defective O-Glycosylation of Thrombospondin Type 1 Repeats
  mā: Daniel Heß, me ētahi atu.
  I whakaputaina: (2008)
• An Unusual Case of Peters Plus Syndrome with Sexual Ambiguity and Absence of Mutations in the B3GALTL Gene
  mā: Siala, Olfa, me ētahi atu.
  I whakaputaina: (2013)
• Novel B3GALTL mutations in classic Peters Plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes
  mā: Weh, Eric, me ētahi atu.
  I whakaputaina: (2013)