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Molecular Identification and Successful Treatment with Targeted Therapy in Gorlin Syndrome A Case Report

Year: 2024

Type: article

Study design: Case Report

Abstract: Gorlin Syndrome (GS), is a rare autosomal dominant cancer predisposition disorder, frequently under diagnosed.

Source: Journal on oncology

DOI: 10.52768/2692-563x/1157

Author: Patricia Esperon

Institution: Universidad de la República de Uruguay

Language: English

Topic: Hedgehog Signaling Pathway Studies

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

OpenAlex ID: W4409848787

FWCI:

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Related to: 10