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Molecular biology / Blindness / Channelopathy / Retinitis pigmentosa / Mutation / Genotyping / Usher syndrome / Exome sequencing / Biology / Genetics / Health


Document Date: 2014-05-21 05:19:57

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Company

The express / ASPER BIOTECH Ltd / /

Currency

EUR / /

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IndustryTerm

Supportive services / /

MedicalCondition

Alström Syndrome / McKusick-Kaufman Syndrome / samples Congenital Stationary Night Blindness APEX / N/A Single mutation Bardet Biedl Syndrome / Chediak-Higashi Syndrome NGS / PAX6 gene Single mutation Autosomal Dominant Optic Atrophy APEX / samples Age-related macular degeneration NGS / samples X-Linked Retinitis Pigmentosa APEX / Borjeson-Forssman-Lehmann Syndrome / genes N/A Single mutation Leber Congenital Amaurosis APEX / genes N/A Single mutation Autosomal Dominant Retinitis Pigmentosa APEX / genes N/A Single mutation Autosomal Recessive Retinitis Pigmentosa APEX / Hermansky-Pudlak
Syndrome / ABCA4 gene N/A Single mutation Usher Syndrome APEX / Ocular Albinism / /

Organization

European Union / /

Person

Rod Dystrophy / /

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Position

Ophthalmics Investigator / ABCA4 gene N/A Single mutation Usher / /

Technology

Genotyping / /

URL

www.asperophthalmics.com / www.asperbio.com_ / http /

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