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Hajrah Sarkar Selected Research

retinol dehydrogenase

1/2020Novel Heterozygous Deletion in Retinol Dehydrogenase 12 (RDH12) Causes Familial Autosomal Dominant Retinitis Pigmentosa.
11/2019Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives.

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Hajrah Sarkar Research Topics

Disease

2Choroideremia
01/2022 - 01/2019
1Aniridia
01/2021
1Microphthalmos
01/2021
1Retinal Dystrophies
01/2020
1Retinitis Pigmentosa (Pigmentary Retinopathy)
01/2020
1Leber Congenital Amaurosis
01/2020
1Retinal Diseases
11/2019
1Neoplasms (Cancer)
05/2015
1African Trypanosomiasis (Nagana)
05/2015

Drug/Important Bio-Agent (IBA)

2retinol dehydrogenaseIBA
01/2020 - 11/2019
1Pharmaceutical PreparationsIBA
01/2021
1Nonsense Codon (Nonsense Mutation)IBA
01/2019
1Mechlorethamine (Nitrogen Mustard)FDA Link
05/2015
1EnzymesIBA
05/2015

Therapy/Procedure

2Therapeutics
01/2022 - 01/2019
1Drug Therapy (Chemotherapy)
05/2015