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A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes.

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Title: A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes.
Authors: Gershlick DC; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA., Ishida M; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA., Jones JR; Greenwood Genetic Center, Greenwood, SC, USA., Bellomo A; Greenwood Genetic Center, Greenwood, SC, USA., Bonifacino JS; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA., Everman DB; Greenwood Genetic Center, Greenwood, SC, USA.
Source: Human molecular genetics [Hum Mol Genet] 2019 May 01; Vol. 28 (9), pp. 1548-1560.
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes.
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  Data: <searchLink fieldCode="AU" term="%22Gershlick+DC%22">Gershlick DC</searchLink>; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Ishida+M%22">Ishida M</searchLink>; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Jones+JR%22">Jones JR</searchLink>; Greenwood Genetic Center, Greenwood, SC, USA.<br /><searchLink fieldCode="AU" term="%22Bellomo+A%22">Bellomo A</searchLink>; Greenwood Genetic Center, Greenwood, SC, USA.<br /><searchLink fieldCode="AU" term="%22Bonifacino+JS%22">Bonifacino JS</searchLink>; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Everman+DB%22">Everman DB</searchLink>; Greenwood Genetic Center, Greenwood, SC, USA.
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2019 May 01; Vol. 28 (9), pp. 1548-1560.
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  Data: Case Reports; Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1093/hmg/ddy423
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              Text: 2019 May 01
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