Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes

✍ Scribed by Weh, E.; Reis, L.M.; Tyler, R.C.; Bick, D.; Rhead, W.J.; Wallace, S.; McGregor, T.L.; Dills, S.K.; Chao, M.-C.; Murray, J.C.; Semina, E.V.

• Book ID: 121409595
• Publisher: John Wiley and Sons
• Year: 2013
• Tongue: English
• Weight: 668 KB
• Volume: 86
• Category: Article
• ISSN: 0009-9163
• DOI: 10.1111/cge.12241