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pro vyhledávání: '"S, Nor Khairullah"'
Publikováno v:
The Medical journal of Malaysia. 77(5)
Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of hereditary disorders in which there is progressive loss of photoreceptors and pigment epithelial function culminating in complete vision loss. Unfortunately, given the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fe97525582da88f3567b8ddf14265b35
https://pubmed.ncbi.nlm.nih.gov/36169067
https://pubmed.ncbi.nlm.nih.gov/36169067
Autor:
Nor Khairullah S; 23 Century International life Science Centre, Seri Kembangan, Selangor, Malaysia. profdatodrnor@23century.my., Nor Fariza N; Hospital Shah Alam, Department of Ophthalmology, Shah Alam, Selangor, Malaysia., Roslin AAZ; Hospital Shah Alam, Department of Ophthalmology, Shah Alam, Selangor, Malaysia., Angelina T; Cellaax Sdn Bhd, Seri Kembangan, Selangor, Malaysia.
Publikováno v:
The Medical journal of Malaysia [Med J Malaysia] 2022 Sep; Vol. 77 (5), pp. 564-568.