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  A family with Axenfeld–Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene
 
 
Title: A family with Axenfeld–Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene
Author: Honkanen, Robert A
Nishimura, Darryl Y
Swiderski, Ruth E
Bennett, Steven R
Hong, Sungpyo
Kwon, Young H
Stone, Edwin M
Sheffield, Val C
Alward, Wallace L.M
Appeared in: American journal of ophthalmology
Paging: Volume 135 (2003) nr. 3 pages 8 p.
Year: 2003
Contents:
Publisher: Elsevier Science Inc.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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