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Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia.

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Title: Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia.
Authors: Seo Y; Department of Ophthalmology, Institute of Vision Research, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, South Korea., Lim HT; Seoul Orthopia Eye Clinic, Seoul, South Korea., Lee BJ; Department of Ophthalmology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea., Han J; Department of Ophthalmology, Institute of Vision Research, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2023 Feb; Vol. 191 (2), pp. 582-585. Date of Electronic Publication: 2022 Nov 11.
Publication Type: Case Reports; Research Support, Non-U.S. Gov't; Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia.
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  Data: <searchLink fieldCode="AU" term="%22Seo+Y%22">Seo Y</searchLink>; Department of Ophthalmology, Institute of Vision Research, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, South Korea.<br /><searchLink fieldCode="AU" term="%22Lim+HT%22">Lim HT</searchLink>; Seoul Orthopia Eye Clinic, Seoul, South Korea.<br /><searchLink fieldCode="AU" term="%22Lee+BJ%22">Lee BJ</searchLink>; Department of Ophthalmology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.<br /><searchLink fieldCode="AU" term="%22Han+J%22">Han J</searchLink>; Department of Ophthalmology, Institute of Vision Research, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2023 Feb; Vol. 191 (2), pp. 582-585. <i>Date of Electronic Publication: </i>2022 Nov 11.
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  Data: Case Reports; Research Support, Non-U.S. Gov't; Journal Article
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE
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        Value: 10.1002/ajmg.a.63037
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      – Code: eng
        Text: English
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      – TitleFull: Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia.
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            NameFull: Seo Y
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            NameFull: Lim HT
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            NameFull: Lee BJ
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            NameFull: Han J
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            – D: 01
              M: 02
              Text: 2023 Feb
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              Y: 2023
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              Value: 191
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            – TitleFull: American journal of medical genetics. Part A
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