A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family.
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| Title: | A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. |
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| Authors: | Berry, Vanita1,2 (AUTHOR) v.berry@ucl.ac.uk, Fujinami, Kaoru1,2,3 (AUTHOR), Mochizuki, Kiyofumi4 (AUTHOR), Iwata, Takeshi5 (AUTHOR), Pontikos, Nikolas1,2 (AUTHOR), Quinlan, Roy A.6 (AUTHOR), Michaelides, Michel1,2 (AUTHOR) michel.michaelides@ucl.ac.uk |
| Source: | Ophthalmic Genetics. Oct2022, Vol. 43 Issue 5, p622-626. 5p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 159359067 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Berry%2C+Vanita%22">Berry, Vanita</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> v.berry@ucl.ac.uk</i><br /><searchLink fieldCode="AR" term="%22Fujinami%2C+Kaoru%22">Fujinami, Kaoru</searchLink><relatesTo>1,2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mochizuki%2C+Kiyofumi%22">Mochizuki, Kiyofumi</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Iwata%2C+Takeshi%22">Iwata, Takeshi</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pontikos%2C+Nikolas%22">Pontikos, Nikolas</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Quinlan%2C+Roy+A%2E%22">Quinlan, Roy A.</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Michaelides%2C+Michel%22">Michaelides, Michel</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> michel.michaelides@ucl.ac.uk</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Ophthalmic+Genetics%22">Ophthalmic Genetics</searchLink>. Oct2022, Vol. 43 Issue 5, p622-626. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=159359067 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1080/13816810.2022.2090010 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 622 Titles: – TitleFull: A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Berry, Vanita – PersonEntity: Name: NameFull: Fujinami, Kaoru – PersonEntity: Name: NameFull: Mochizuki, Kiyofumi – PersonEntity: Name: NameFull: Iwata, Takeshi – PersonEntity: Name: NameFull: Pontikos, Nikolas – PersonEntity: Name: NameFull: Quinlan, Roy A. – PersonEntity: Name: NameFull: Michaelides, Michel IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: Oct2022 Type: published Y: 2022 Identifiers: – Type: issn-print Value: 13816810 Numbering: – Type: volume Value: 43 – Type: issue Value: 5 Titles: – TitleFull: Ophthalmic Genetics Type: main |
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