Search Results - Vaishali Chanpura
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Rare Coexistence of SLC6A9 and TOR1A Gene Mutations in a Neonate Presenting with Hereditary Hyperekplexia and Arthrogryposis Multiplex Congenita: A Case Report with Review of Liter... by Bhavya Patel, Shwetal Bhatt, Vaishali Chanpura
Published 2023Call Number: Loading…Connect to this object online.
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