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Kearns L 1

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58892 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; Ruddle JB; Ali H; Carnt N; Gardner JC; Hassan H; Gade E; Kearns L; Jelsig AM; Restori M; Webb TR; Laws D; Cosgrove M; Hertz JM; Russell-Eggitt I; Pilz DT; Hammond CJ; Tuft SJ; Hardcastle AJ
PLoS ONE 2014; 9: e104163

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