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Macular dystrophy in Heimler syndrome

  • Published:2011-03-02 Issue:2 Volume:32 Page:97-100
  • ISSN:1381-6810
  • Container-title:Ophthalmic Genetics
  • language:en
  • Short-container-title:Ophthalmic Genetics

Author:

Lima Luiz H.,Barbazetto Irene A.,Chen Royce,Yannuzzi Lawrence A.,Tsang Stephen H.,Spaide Richard F.

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Cited by 19 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heimler syndrome with a complaint of blurred vision caused by compound heterozygous variants in PEX1;European Journal of Ophthalmology;2024-03-15

2. Ophthalmic Manifestations of Heimler Syndrome in Two Siblings With PEX1 Variants;Journal of Pediatric Ophthalmology & Strabismus;2024-01

3. A novel compound heterozygous PEX1 variant in Heimler syndrome;Experimental Eye Research;2023-12

4. Ocular Manifestations in Patients with Sensorineural Hearing Loss;Journal of Ophthalmic and Vision Research;2022-11-24

5. Dysfunctional peroxisomal lipid metabolisms and their ocular manifestations;Frontiers in Cell and Developmental Biology;2022-09-07
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