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Clinical and Molecular Investigations Into Ciliopathies

Source: ClinicalTrials.gov – Retinitis Pigmentosa – Clinical and Molecular Investigations Into Ciliopathies


Conditions:   Autosomal Recessive Polycystic Kidney Disease;   Congenital Hepatic Fibrosis;   Caroli’s Disease;   Polycystic Kidney Disease;   Joubert Syndrome;   Cerebro-Oculo-Renal Syndromes;   COACH Syndrome;   Senior-Loken Syndrome;   Dekaban-Arima Syndrome;   Cogan Oculomotor Apraxia;   Nephronophthisis;   Bardet-Biedl Syndrome;   Alstrom Syndrome;   Oral-Facial-Digital Syndrome
Intervention:  
Sponsor:   National Human Genome Research Institute (NHGRI)
Recruiting – verified June 30, 2017


Source: ClinicalTrials.gov – Retinitis Pigmentosa – Clinical and Molecular Investigations Into Ciliopathies

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