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A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures
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2011 (English)In: Human Molecular Genetics, ISSN 0964-6906, E-ISSN 1460-2083, Vol. 20, no 10, p. 1886-1892Article in journal (Refereed) Published
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2011. Vol. 20, no 10, p. 1886-1892
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Medical Genetics and Genomics
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URN: urn:nbn:se:uu:diva-468508DOI: 10.1093/hmg/ddr070OAI: oai:DiVA.org:uu-468508DiVA, id: diva2:1648028
Available from: 2022-03-29 Created: 2022-03-29 Last updated: 2025-02-10

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