Challenges of Phenotype-Genotype Correlations in Rare Diseases-Reply

JAMA Ophthalmol. 2021 Dec 1;139(12):1323-1324. doi: 10.1001/jamaophthalmol.2021.4375.

Authors

Vasily M Smirnov^{1

2

3}, Christina Zeitz¹, Isabelle Audo^{1

4

5}

Affiliations

¹ Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
² Université de Lille, Faculté de Médecine, Lille, France.
³ Exploration de la Vision et Neuro-Ophtalmologie, CHU de Lille, Lille, France.
⁴ Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, INSERM-DHOS CIC 1423, Paris, France.
⁵ Institute of Ophthalmology, University College London, London, United Kingdom.

PMID: 34709364
DOI: 10.1001/jamaophthalmol.2021.4375

No abstract available

Publication types

Letter
Comment

MeSH terms

Genetic Association Studies
Genotype
Humans
Phenotype
Rare Diseases* / genetics