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Predicting the pathogenicity of NKX2-1 and IGSF1 variants with in silico bioinformatic tools

Satoshi Narumi1

  • 1Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.

Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology
|July 23, 2020
PubMed
Abstract

No abstract available in PubMed .

Keywords:
IGSF1NKX2-1congenital hypothyroidismgeneticsin silicomutation

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