Axenfeld-Rieger syndrome: A systematic review examining genetic, neurological, and neurovascular associations to inform screening

Author:

Muzyka LoganORCID,Winterhalter EmilyORCID,LoPresti Melissa A.,Scoville Jonathan,Bohnsack Brenda L.ORCID,Lam Sandi K.ORCID

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference77 articles.

1. Axenfeld-Rieger syndrome;Seifi;Clin. Genet.,2018

2. Axenfeld-Rieger syndrome: a theory of mechanism and distinctions from the iridocorneal endothelial syndrome;Shields;Trans. Am. Ophthalmol. Soc.,1983

3. Ophthalmological features associated with COL4A1 mutations;Coupry;Arch. Ophthalmol.,2010

4. Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease;French;J. Clin. Invest.,2014

5. Mechanistic insights into Axenfeld–Rieger syndrome from zebrafish foxc1 and pitx2 mutants;French;Int. J. Mol. Sci.,2021

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