Microvillus Inclusion Disease: A Rare Mutation of STX3 in Exon 9 Causing Fatal Congenital Diarrheal Disease
Pournami, Femitha, MK, Alok Kumar, Panackal, Anila V., Nandakumar, Anand, Prabhakar, Jyothi, Jain, Naveen
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.06.2022)
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.06.2022)
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