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Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness
Davidson AE,
Cheong SS,
Hysi PG,
Venturini C,
Plagnol V,
et al.
(2014)
Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness.
PLOS ONE 9(8): e104163.
https://doi.org/10.1371/journal.pone.0104163