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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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HbE-Beta Thalassemia with Moyamoya Syndrome: A Rare Association
Anika Agrawal1, Onkar Singh Bhinder2, Devendra Mishra2
1Department of Pediatrics, Maulana Azad Medical College, New Delhi, 110002, India. dranikaagrawal@gmail.com.
Indian Journal of Pediatrics
|December 22, 2019
Abstract
No abstract available in PubMed .
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