DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Vogt G, Kádasi ĽL, Czeizel E.
Homozygous E387K (1159G>A) mutation of the CYP1B1 gene in a Roma boy affected with primary congenital glaucoma. Case report [in Hungarian].
Orv Hetil 2014;
155 (33) 1325-1328
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