Stargardt disease and progress in therapeutic strategies

D Huang, RC Heath Jeffery, MT Aung-Htut… - Ophthalmic …, 2022 - Taylor & Francis
Background Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy due to
mutations in ABCA4, characterized by subretinal deposition of lipofuscin-like substances …
被引用次数：28 相关文章
[PDF] researchgate.net

[PDF][PDF] Stargardt disease and progress in therapeutic strategies

D Huang, RCH Jeffery, MT Aung-Htut, S McLenachan… - 2021 - researchgate.net
ABSTRACT Background: Stargardt disease (STGD1) is an autosomal recessive retinal
dystrophy due to mutations in ABCA4, characterized by subretinal deposition of lipofuscin …

Stargardt disease and progress in therapeutic strategies

D Huang, RCH Jeffery, MT Aung-Htut… - Ophthalmic …, 2022 - pubmed.ncbi.nlm.nih.gov
Background Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy due to
mutations in ABCA4, characterized by subretinal deposition of lipofuscin-like substances …

Stargardt disease and progress in therapeutic strategies

D Huang, RCH Jeffery… - Ophthalmic …, 2022 - research-repository.uwa.edu.au
Background: Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy due to
mutations in ABCA4, characterized by subretinal deposition of lipofuscin-like substances …

Stargardt disease and progress in therapeutic strategies.

D Huang, HJ RC, MT Aung-Htut… - Ophthalmic …, 2021 - europepmc.org
Background Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy due to
mutations in ABCA4, characterized by subretinal deposition of lipofuscin-like substances …
[PDF] murdoch.edu.au

[PDF][PDF] Stargardt disease and progress in therapeutic strategies

D Huang, RC Heath Jeffery, MT Aung-Htut - 2021 - researchportal.murdoch.edu.au
ABSTRACT Background: Stargardt disease (STGD1) is an autosomal recessive retinal
dystrophy due to mutations in ABCA4, characterized by subretinal deposition of lipofuscin …

Stargardt disease and progress in therapeutic strategies

D Huang, RCH Jeffery… - Ophthalmic …, 2021 - researchportal.murdoch.edu.au
Background: Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy due to
mutations in ABCA4, characterized by subretinal deposition of lipofuscin-like substances …