[HTML][HTML] Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review
BA Othman, JE Ong, AV Dumitrescu - Genes, 2022 - mdpi.com
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review.
BA Othman, JE Ong, AV Dumitrescu - Genes, 2022 - search.ebscohost.com
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
Biallelic Optic Atrophy 1 (OPA1) Related Disorder-Case Report and Literature Review
B Al Othman, JE Ong, AV Dumitrescu - Genes, 2022 - iro.uiowa.edu
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review
B Al Othman, JE Ong, AV Dumitrescu - Genes, 2022 - agris.fao.org
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
Biallelic Optic Atrophy 1 (OPA1) Related Disorder-Case Report and Literature Review.
BA Othman, JE Ong, AV Dumitrescu - Genes, 2022 - europepmc.org
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
[PDF][PDF] Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review. Genes 2022, 13, 1005
BA Othman, JE Ong, AV Dumitrescu - 2022 - pdfs.semanticscholar.org
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
Biallelic Optic Atrophy 1 (OPA1) Related Disorder-Case Report and Literature Review
B Al Othman, JE Ong, AV Dumitrescu - Genes, 2022 - pubmed.ncbi.nlm.nih.gov
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
[HTML][HTML] Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review
B Al Othman, JE Ong, AV Dumitrescu - Genes, 2022 - ncbi.nlm.nih.gov
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review
B Al Othman, JE Ong, AV Dumitrescu - Genes, 2022 - search.proquest.com
Dominant optic atrophy (DOA), MIM# 605290, is the most common hereditary optic
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …
neuropathy inherited in an autosomal dominant pattern. Clinically, it presents a progressive …