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CODE Think! Rare Mutations of STX3 Causing Microvillus Inclusion Disease.
Elizabeth Mary John
Sajina Sathyan
Femitha Pournami
Ajai Kumar Prithvi
Anand Nandakumar
Jyothi Prabhakar
Naveen Jain
Published in:
Journal of pediatric genetics (2023)
Keyphrases
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