A carregar...
Expanding Phenotype of VRK1 Mutations in Motor Neuron Disease
OBJECTIVE: In the past decade, hereditary forms of motor neuron disease (spinal muscular atrophy and/or amyotrophic lateral sclerosis) are increasingly identified. As advanced genetic testing is performed, molecular diagnosis can be obtained. Identifying new gene mutations can lead to further unders...
Na minha lista:
| Publicado no: | J Clin Neuromuscul Dis |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4829393/ https://ncbi.nlm.nih.gov/pubmed/26583493 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/CND.0000000000000096 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|