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A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene |
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| Authors: | 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 |
| Affiliation: | Department of Ophthalmology, Howard Hughes Medical Institute, The University of Iowa, Iowa City, Iowa, USA. |
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| 本文献已被 ScienceDirect PubMed 等数据库收录！ | |