Work

Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner–Hanhart Syndrome

Year: 2013

Type: article

Study design: Case Report

Source: Gene

DOI: 10.1016/j.gene.2013.07.066

Authors: Yosra Bouyacoub, Hela Zribi, Hatem Azzouz, Fehmi Nasrallah, Rim Ben Abdelaziz, Monia Kacem, Ben Rekaya, Olfa Messaoud, Lilia Romdhane, Cherine Charfeddine, Mustapha Bouziri, Sonia Bouziri, Neji Tebib, Mourad Mokni, Naziha Kaabachi, Samir Boubaker, Sonia Abdelhak

Institutions: University of Monastir, Institut Pasteur de Tunis, Tunis El Manar University, Hôpital La Rabta

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

Funder: Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche

OpenAlex ID: W2000717442

FWCI: 0.222

Cites: 43

Cited by: 14

Related to: 10