Results
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6261.
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6262.
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6263.
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Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness. [electronic resource] by
- Zeitz, Christina
- Kloeckener-Gruissem, Barbara
- Forster, Ursula
- Kohl, Susanne
- Magyar, István
- Wissinger, Bernd
- Mátyás, Gábor
- Borruat, François-Xavier
- Schorderet, Daniel F
- Zrenner, Eberhart
- Munier, Francis L
- Berger, Wolfgang
Producer: 20061031
In:
American journal of human genetics vol. 79
Availability: No items available.
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6264.
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6265.
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6266.
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CRYBA4, a novel human cataract gene, is also involved in microphthalmia. [electronic resource] by
- Billingsley, Gail
- Santhiya, Sathiyavedu T
- Paterson, Andrew D
- Ogata, Koji
- Wodak, Shoshana
- Hosseini, S Mohsen
- Manisastry, Shyam Manohar
- Vijayalakshmi, Perumalsamy
- Gopinath, Pudhiya Mundyat
- Graw, Jochen
- Héon, Elise
Producer: 20061031
In:
American journal of human genetics vol. 79
Availability: No items available.
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6267.
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6268.
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6269.
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6270.
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6271.
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6272.
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6273.
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6274.
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6275.
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6276.
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6277.
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6278.
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6279.
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6280.
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