Results
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5361.
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5362.
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5363.
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5364.
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5365.
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5366.
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Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration. [electronic resource] by
- Lewis, C A
- Batlle, I R
- Batlle, K G
- Banerjee, P
- Cideciyan, A V
- Huang, J
- Alemán, T S
- Huang, Y
- Ott, J
- Gilliam, T C
- Knowles, J A
- Jacobson, S G
Producer: 19990811
In:
Investigative ophthalmology & visual science vol. 40
Availability: No items available.
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5367.
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5368.
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5369.
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5371.
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5372.
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Transient photoreceptor deconstruction by CNTF enhances rAAV-mediated cone functional rescue in late stage CNGB3-achromatopsia. [electronic resource] by
- Komáromy, András M
- Rowlan, Jessica S
- Corr, Amanda T Parton
- Reinstein, Shelby L
- Boye, Sanford L
- Cooper, Ann E
- Gonzalez, Amaliris
- Levy, Britt
- Wen, Rong
- Hauswirth, William W
- Beltran, William A
- Aguirre, Gustavo D
Producer: 20140207
In:
Molecular therapy : the journal of the American Society of Gene Therapy vol. 21
Availability: No items available.
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5373.
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Diagnostic fundus autofluorescence patterns in achromatopsia. [electronic resource] by
- Fahim, Abigail T
- Khan, Naheed W
- Zahid, Sarwar
- Schachar, Ira H
- Branham, Kari
- Kohl, Susanne
- Wissinger, Bernd
- Elner, Victor M
- Heckenlively, John R
- Jayasundera, Thiran
Producer: 20140115
In:
American journal of ophthalmology vol. 156
Availability: No items available.
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5374.
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Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene. [electronic resource] by
- Felden, Julia
- Baumann, Britta
- Ali, Manir
- Audo, Isabelle
- Ayuso, Carmen
- Bocquet, Beatrice
- Casteels, Ingele
- Garcia-Sandoval, Blanca
- Jacobson, Samuel G
- Jurklies, Bernhard
- Kellner, Ulrich
- Kessel, Line
- Lorenz, Birgit
- McKibbin, Martin
- Meunier, Isabelle
- de Ravel, Thomy
- Rosenberg, Thomas
- Rüther, Klaus
- Vadala, Maria
- Wissinger, Bernd
- Stingl, Katarina
- Kohl, Susanne
Producer: 20200330
In:
Human mutation vol. 40
Availability: No items available.
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5375.
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5380.
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