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LDRTC is a non-profit organization founded in 2013 by Dr. Ozlem Goker-Alpan with a vision to provide high-quality care for individuals with lysosomal storage diseases and other rare genetic disorders. Dr. Ozlem Goker-Alpan is a world-renowned authority in the field of lysosomal and other rare genetic disorders and is well known for her dedication to the health and well-being of her patients and families. Our Goal: LDRTC utilizes a variety of clinical treatment and research protocols, conducts training programs to increase awareness, and offers compassionate care and a platform for the patients and families affected by these debilitating disorders. Our...
Lysosomal storage diseases,gaucher disease,fabry disease,pompe disease,rare diseases,enzyme replacement therapy,substrate reduction therapy,inherited metabolic disorders,niemann pick disease,mucopolysaccharidosis,genetic diseases,bone disease,lysosomal storage disorders,and autophagy
Lysosomal and rare disorders research and treatment center (ldrtc) operates in the Non-profit organization management industry.
Lysosomal and rare disorders research and treatment center (ldrtc)'s revenue is 11m - 100m
Lysosomal and rare disorders research and treatment center (ldrtc) has 11 - 50 employees.
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