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Ciliopathy: Alström Syndrome

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Atlas of Inherited Retinal Diseases

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 1085))

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Suggested Reading

  • Chen JH, Geberhiwot T, Barrett TG, Paisey R, Semple RK. Refining genotype-phenotype correlation in Alstrom syndrome through study of primary human fibroblasts. Mol Genet Genomic Med. 2017;15:390–404.

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Authors and Affiliations

  1. Jonas Children’s Vision Care, Bernard & Shirlee Brown Glaucoma Laboratory, Columbia Stem Cell Initiative-Departments of Ophthalmology, Biomedical Engineering, Pathology & Cell Biology, Institute of Human Nutrition, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA

    Stephen H. Tsang

  2. Department of Ophthalmology, Columbia University, Edward S. Harkness Eye Institute, NewYork-Presbyterian Hospital, New York, NY, USA

    Stephen H. Tsang & Tarun Sharma

  3. Department of Pediatrics, Division of Genetics, University of California San Francisco, San Francisco, CA, USA

    Alicia R. P. Aycinena

Authors
  1. Stephen H. Tsang
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  2. Alicia R. P. Aycinena
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  3. Tarun Sharma
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Corresponding authors

Correspondence to Alicia R. P. Aycinena or Tarun Sharma .

Editor information

Editors and Affiliations

  1. Jonas Children’s Vision Care, Bernard & Shirlee Brown Glaucoma Laboratory, Columbia Stem Cell Initiative-Departments of Ophthalmology, Biomedical Engineering, Pathology & Cell Biology, Institute of Human Nutrition, Vagelos College of Physicians and Surgeons Columbia University, New York, NY, USA

    Stephen H. Tsang

  2. Department of Ophthalmology, Edward S. Harkness Eye Institute NewYork-Presbyterian Hospital Columbia University, New York, NY, USA

    Tarun Sharma

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© 2018 Springer International Publishing AG, part of Springer Nature

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Tsang, S.H., Aycinena, A.R.P., Sharma, T. (2018). Ciliopathy: Alström Syndrome. In: Tsang, S., Sharma, T. (eds) Atlas of Inherited Retinal Diseases. Advances in Experimental Medicine and Biology, vol 1085. Springer, Cham. https://doi.org/10.1007/978-3-319-95046-4_35

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