Mutations in KARS Cause a Severe Neurological and Neurosensory Disease With Optic Neuropathy

Human Mutation - United States
doi 10.1002/humu.23799
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Wiley

Related search

Mutations in XRCC1 Cause Cerebellar Ataxia and Peripheral Neuropathy

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
2018English

Periaxin Mutations Cause Recessive Dejerine-Sottas Neuropathy

American Journal of Human Genetics
Genetics
2001English

Bi-Allelic ADPRHL2 Mutations Cause Neurodegeneration With Developmental Delay, Ataxia, and Axonal Neuropathy

American Journal of Human Genetics
Genetics
2018English

Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

American Journal of Human Genetics
Genetics
2013English

Contour Variability in Thyroid Eye Disease With Compressive Optic Neuropathy Treated With Radiotherapy

Advances in Radiation Oncology
Nuclear MedicineRadiologyImagingOncology
2020English

Severe, Early Axonal Degeneration Following Experimental Anterior Ischemic Optic Neuropathy

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2014English

Leber's Hereditary Optic Neuropathy-Not Just a Young Men's Disease

Journal of the American Geriatrics Society
GerontologyGeriatrics
2016English

Optic Neuropathy

2018English

Progressive Auditory Neuropathy in Patients With Leber's Hereditary Optic Neuropathy

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
2004English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy