This website provides information on patients with mutations in the LINS1 gene, including clinical data, molecular data, its management and research options.

Intellectual developmental disorder, autosomal recessive 27, is due to mutations in the LINS1 gene. It is characterized by delayed psychomotor development, poor speech and hyperreflexia. Some patients present with microcephaly and aggressive behavior.

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the LINS1 gene.

Jayesh Sheth, PhD, FRIGE’s Institute of Human Genetics, Ahmedabad, India, jayesh.sheth@frige.co.in

Aadhira Nair, MSc, FRIGE’s Institute of Human Genetics, Ahmedabad, India, aadhira.nair@frige.co.in

Harsh Sheth, PhD, FRIGE’s Institute of Human Genetics, Ahmedabad, India, riddhi.bhavsar@frige.co.in

Frenny Sheth, PhD, FRIGE’s Institute of Human Genetics, Ahmedabad, India, harsh.sheth@frige.co.in