Identification of a novel variant in EARS2 associated with a severe clinical phenotype expands the clinical spectrum of LTBL

1. Barbosa-Gouveia, S.
2. González-Vioque, E.
3. Hermida, Á.
4. Suarez, M.U.
5. Martínez-González, M.J.
6. Borges, F.
7. Wintjes, L.
8. Kappen, A.
9. Rodenburg, R.
10. Couce, M.-L.

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DOI: 10.3390/GENES11091028 GOOGLE SCHOLAR lock_openOpen access editor

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