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Jain Foundation - Dysferlin Registry - LGMD2B/R2 - DYSFERLINOPATHY - MIYOSHI MYOPATHY 1
ORCHESTRATING A CURE FOR DYSFERLINOPATHY The Jain Foundation is singularly focused on finding a cure for dysferlinopathy, also referred to as LGMD2B, LGMDR2, Miyoshi Myopathy 1 LEARN MORE O...
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Our Mission - Jain Foundation
ABOUT Our Mission ABOUT Our Mission Home ❯ About ❯ Our Mission Our Mission The Jain Foundation is a non-profit disease foundation established by Ajit Jain of Berkshire H...
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LGMD Facts | Jain Foundation
LGMD Facts Many of the facts listed below about LGMDs apply to these closely related diseases such as Pompe, FSHD (Facioscapulohumeral muscular dystrophy) and HIBM (Hereditary inclusion body myopathie...
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Application of Rosetta and Foldit for Structural Modeling of DYSF - Jain Foundation
Grant Duration 06/16 - 05/17 Autosomal recessive mutations in the human gene encoding the dysferlin protein (DYSF) are the cause of rare forms of muscular dystrophies known as dysferlinopathies,...
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Merit-Based Scholarship | Jain Foundation
The application includes two short essay questions. Applications must be submitted by Wednesday, May 25, 2016 at 12:00am PDT. History of academic success Proof of spreading disease awareness to 25-1...
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What is Miyoshi Myopathy? | Jain Foundation
Home[1] > What is Miyoshi Myopathy? Myopathy simply means...