A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome

Authors

Yuqing Song

Published

November 1, 2024

Abstract

Functional defects caused by mutations in the insulin receptor (INSR) gene often lead to severe hereditary insulin resistance syndromes, including but not limited to type A insulin resistance syndrome.

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Journal

Diabetes Metabolic Syndrome and Obesity

Topics

DOI

10.2147/dmso.s481745

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CC-BY-NC

A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome

Authors

Yuqing Song

Published

November 1, 2024

Abstract

Supporters

Support the authors with ResearchCoin

Journal

Diabetes Metabolic Syndrome and Obesity

Topics

DOI

10.2147/dmso.s481745

License

CC-BY-NC

Paper

Paper

Paper

Paper

A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome

Abstract

Supporters

Journal

Topics

DOI

License

A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome

Abstract

Supporters

Journal

Topics

DOI

License

Supporters

Journal

Topics

DOI

License