TY  - GEN
AU  - Seifi,Morteza
AU  - Footz,Tim
AU  - Taylor,Sherry A M
AU  - Elhady,Ghada M
AU  - Abdalla,Ebtesam M
AU  - Walter,Michael A
TI  - Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
SN  - 1755-3768
PY  - 2017///0125
KW  - Adult
KW  - Anterior Eye Segment
KW  - abnormalities
KW  - Child, Preschool
KW  - Consanguinity
KW  - DNA Copy Number Variations
KW  - DNA Mutational Analysis
KW  - Exons
KW  - genetics
KW  - Eye Abnormalities
KW  - Eye Diseases, Hereditary
KW  - Homeodomain Proteins
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Open Reading Frames
KW  - Pedigree
KW  - Real-Time Polymerase Chain Reaction
KW  - Sequence Deletion
KW  - Transcription Factors
KW  - Homeobox Protein PITX2
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1111/aos.13030
ER  -