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

AuthID
P-00Z-CKR
Document Type
Article
Year published
2023
Published
in Case Reports in Ophthalmology, ISSN: 1663-2699
Pages: 519-527 (8)
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Publication Identifiers
Scopus: 2-s2.0-85176581559
Source Identifiers
ISSN: 1663-2699
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