<i>TARDBP</i> Mutations in Facial-Onset Sensory and Motor Neuronopathy-Reference-Cited by-同舟云学术

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TARDBP Mutations in Facial-Onset Sensory and Motor Neuronopathy

Published:2024-06 Issue:3 Volume:10 Page:
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Picher-Martel Vincent¹^ORCID,Babu Suma¹^ORCID,Amato Anthony A.¹^ORCID

Affiliation:

1. From the Department of Neurology (V.P.-M.), Massachusetts General Hospital/Harvard Medical School; Department of Neurology (V.P.-M.), MassGeneral Institute for Neurodegenerative Diseases (MIND); Department of Neurology (S.B.), Massachusetts General Hospital; Department of Neurology (A.A.A.), Brigham Women's Hospital, Harvard Medical School, Boston, MA.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Link

https://www.neurology.org/doi/pdfdirect/10.1212/NXG.0000000000200160

Reference15 articles.

1. Facial onset sensory and motor neuronopathy (FOSMN syndrome): Cases series and systematic review

2. Facial Onset Sensory Motor Neuronopathy

3. Facial onset sensory and motor neuronopathy (FOSMN) syndrome responding to immunotherapies

4. TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: An autopsied case report and a review of the literature

5. TDP43 pathology in the brain, spinal cord, and dorsal root ganglia of a patient with FOSMN

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