MFN2
MFN2 est un gène situé sur le chromosome 1 humain[5].
Maladies liées
- Neuropathie axonale sévère précoce par déficit en MFN2
- Neuropathie sensitivo-motrice héréditaire type 6[6]
- Maladie de Charcot-Marie-Tooth autosomique dominante type 2A2
- Neuropathie sensitivo-motrice héréditaire type 5
- Adénolipomatose symétrique à prédominance cervicale
Notes et références
- GRCh38: Ensembl release 89: ENSG00000116688 - Ensembl, May 2017
- GRCm38: Ensembl release 89: ENSMUSG00000029020 - Ensembl, May 2017
- ↑ « Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
- ↑ « Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine
- ↑ (en-US) « Entry - *608507 - MITOFUSIN 2; MFN2 - OMIM - (OMIM.ORG) », sur omim.org (consulté le )
- ↑ « Orphanet: MFN2-mitofusin 2 », sur www.orpha.net (consulté le )
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