Nalaganje...
Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11
OBJECTIVE: Identification of causative mutations in 3 consanguineous families (with 4 affected members) referred to our center with young-onset motor neuron disease and overlapping phenotypes resembling autosomal recessive juvenile amyotrophic lateral sclerosis (ARJALS) and autosomal recessive hered...
Shranjeno v:
| izdano v: | Neurol Genet |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Wolters Kluwer
2015
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4809458/ https://ncbi.nlm.nih.gov/pubmed/27066562 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000025 |
| Oznake: |
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