Editorial & Opinion
Correspondence.
العنوان: | Correspondence. |
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المؤلفون: | Boon CJ; Department of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands †The Rotterdam Eye Hospital, Rotterdam, the Netherlands ‡Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands §Department of Clinical and Molecular Ophthalmogenetics, Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, the Netherlands ¶Department of Ophthalmology, Academic Medical Centre, Amsterdam, the Netherlands **Bartiméus Institute for the Visually Impaired, Zeist, the Netherlands., van den Born LI, Keunen JE, Bergen AA, Riemslag FC, Florijn RJ, van Schooneveld MJ |
المصدر: | Retina (Philadelphia, Pa.) [Retina] 2015 Sep; Vol. 35 (9), pp. e57-8. |
نوع المنشور: | Letter; Comment |
اللغة: | English |
بيانات الدورية: | Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8309919 Publication Model: Print Cited Medium: Internet ISSN: 1539-2864 (Electronic) Linking ISSN: 0275004X NLM ISO Abbreviation: Retina Subsets: MEDLINE |
أسماء مطبوعة: | Publication: Hagerstown, MD : Lippincott Williams & Wilkins Original Publication: Philadelphia : Lippincott, [1981?- |
مواضيع طبية MeSH: | Mutation*, Chloride Channels/*genetics , Eye Diseases, Hereditary/*genetics , Eye Proteins/*genetics , Retinal Diseases/*genetics, Humans |
التعليقات: | Comment on: Retina. 2015 Apr;35(4):773-82. (PMID: 25545482) Comment in: Retina. 2015 Sep;35(9):e58. (PMID: 26312453) |
المشرفين على المادة: | 0 (Chloride Channels) 0 (Eye Proteins) |
تواريخ الأحداث: | Date Created: 20150828 Date Completed: 20151103 Latest Revision: 20181202 |
رمز التحديث: | 20231215 |
DOI: | 10.1097/IAE.0000000000000696 |
PMID: | 26312452 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1539-2864 |
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DOI: | 10.1097/IAE.0000000000000696 |