Work

A novel homozygous mutation causing hereditary tyrosinemia type I in yakut patient in russia: case report.

Year: 2016

Type: article

Study design: Case Report

Source: PubMed

Authors: Nadezda R Maksimova, Elizaveta E Gurinova, Aitalina L Sukhomyasova, Anastasia L Danilova, Vladimir S Kaimonov, Mira T Savvina, Aleksandra E Yakovleva, Elena I Alekseeva

Institution: North-Eastern Federal University

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2518461549

FWCI: 0.255

Cites:

Cited by: 1

Related to: 10