Cohen Syndrome: Novel Vps13B Genetic Variants in a Male Portuguese Patient with Pigmentary Retinopathy

AuthID
 P-00Z-CKR
6
Author(s)
Quental, R
·
Estrela-Silva, S
Tipo de Documento
Article
Year published
2023
Publicado
in CASE REPORTS IN OPHTHALMOLOGY, ISSN: 1663-2699
Volume: 14, Número: 1, Páginas: 519-527 (9)
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Scopus®
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Pubmed®
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Publication Identifiers
Pubmed: 37901634
SCOPUS: 2-s2.0-85176581559
Wos: WOS:001220490000110
Source Identifiers
ISSN: 1663-2699
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