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[HTML][HTML] Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati, A Ciolfi… - Orphanet journal of rare …, 2017 - Springer
Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …
被引用次数：50 相关文章

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati, A Ciolfi… - Orphanet Journal of …, 2017 - infona.pl
Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …
[PDF] academia.edu

[PDF][PDF] Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati, A Ciolfi… - 2017 - academia.edu
Background: Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati, A Ciolfi… - … JOURNAL OF RARE …, 2017 - air.unimi.it
BACKGROUND: Heterozygous mutations in OPA1 are a common cause of autosomal
dominant optic atrophy, sometimes associated with extra-ocular manifestations. Few cases …

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati, A Ciolfi… - … JOURNAL OF RARE …, 2017 - boa.unimib.it
Background: Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations.

A Nasca, T Rizza, M Doimo, A Legati… - Orphanet Journal of …, 2017 - search.ebscohost.com
Abstract < bold> Background: </bold> Heterozygous mutations in OPA1 are a
common cause of autosomal dominant optic atrophy, sometimes associated with extra …
[PDF] researchgate.net

[PDF][PDF] Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati, A Ciolfi… - 2017 - researchgate.net
Background: Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations.

A Nasca, T Rizza, M Doimo, A Legati… - Orphanet Journal of …, 2017 - europepmc.org
Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati… - Orphanet journal of …, 2017 - pubmed.ncbi.nlm.nih.gov
Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …
[PDF] core.ac.uk

[PDF][PDF] Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

A Nasca, T Rizza, M Doimo, A Legati, A Ciolfi… - 2017 - core.ac.uk
Background: Heterozygous mutations in OPA1 are a common cause of autosomal dominant
optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring …