Cyp1B1 Mutational Screening in a Portuguese Cohort of Primary Congenital Glaucoma Patients

AuthID
 P-00M-PXN
7
Author(s)
Carmona, S
·
Roberts, R
·
Wainwright, G
·
Tipo de Documento
Letter
Year published
2017
Publicado
in OPHTHALMIC GENETICS, ISSN: 1381-6810
Volume: 38, Número: 2, Páginas: 197-199 (3)
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Publication Identifiers
Wos: WOS:000399550400021
Source Identifiers
ISSN: 1381-6810
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