This study is currently not recruiting participants.

Molecular Mechanism of Lowe Syndrome and Retinitis Pigmentosa

Not Recruiting
100 years or below
All
Phase N/A
1 Location

Brief description of study.

The purpose of this study is to characterize genetic and molecular defects causing Lowe syndrome and Retinitis Pigmentosa (RP).

Detailed description of study

The purpose of this study is to characterize genetic and molecular defects causing Lowe syndrome and Retinitis Pigmentosa (RP).

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Lowe syndrome,retinitis pigmentosa
  • Age: 100 years or below
  • Gender: All
Updated on 13 Jul 2016. Study ID: 1107006245

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