학술논문

Recurrent "outsider" intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb.
Document Type
Article
Source
Frontiers in Genetics; 2024, p1-7, 7p
Subject
ATROPHY
LIPOIC acid
MOTOR neuron diseases
GENETIC counseling
CONSANGUINITY
BLOOD coagulation factor XIII
Language
ISSN
16648021
Abstract
Copyright of Frontiers in Genetics is the property of Frontiers Media S.A. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)