CODE Think! Rare Mutations of STX3 Causing Microvillus Inclusion Disease

J Pediatr Genet. 2023 Aug 10;12(4):352. doi: 10.1055/s-0043-1772207. eCollection 2023 Dec.

Authors

Elizabeth Mary John¹, Sajina Sathyan¹, Femitha Pournami¹, Ajai Kumar Prithvi¹, Anand Nandakumar¹, Jyothi Prabhakar¹, Naveen Jain¹

Affiliation

¹ Department of Neonatology, Kerala Institute of Medical Sciences, Trivandrum, Kerala, India.

PMID: 38162158
PMCID: PMC10756714 (available on 2024-08-10)
DOI: 10.1055/s-0043-1772207

No abstract available

Grants and funding

Funding None.