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Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

Nature Genetics volume 18, pages 11–12 (1998)Cite this article

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Author information

Author notes

  1. Roser Gonzàlez-Duarte: A.M. -M. and E.P. contributed equally to this work, e-mail: roser@porthos.bio.ub.es

Affiliations

  1. Departament de Genètica, Facultat de Biologia, Universitat de Barcelona, E-08071, Spain

    Amalia Martínez-Mir, Eva Paloma, Lluísa Vilageliu, Roser Gonzàlez-Duarte & Susana Balcells

  2. lntramural Research Support Program,SAIC-Frederick, NCI-Frederick Cancer Research and Development Center, Frederick, Maryland, 21702, USA

    Rando Allikmets

  3. Departamento de Genètica, Fundación Jiménez Díaz, Madrid, E-28040, Spain

    Carmen Ayuso & Teresa del Río

  4. Laboratory of Genomic Diversity, NCI-Frederick Cancer Research and Development Center, Frederick, Maryland, 21702, USA

    Michael Dean

Authors
  1. Amalia Martínez-Mir
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  2. Eva Paloma
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  3. Rando Allikmets
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  4. Carmen Ayuso
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  5. Teresa del Río
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  6. Michael Dean
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  7. Lluísa Vilageliu
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  8. Roser Gonzàlez-Duarte
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  9. Susana Balcells
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Martínez-Mir, A., Paloma, E., Allikmets, R. et al. Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR. Nat Genet 18, 11–12 (1998). https://doi.org/10.1038/ng0198-11

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  • DOI: https://doi.org/10.1038/ng0198-11

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