Publication | Open Access
TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy
100
Citations
17
References
2009
Year
Is MutatedNeurodegenerative DiseasesMendelian DisorderOphthalmologyGenetic DisorderGeneticsLeber Hereditary Optic NeuropathyMolecular GeneticsMitochondrial ProteinMedicine
| Year | Citations | |
|---|---|---|
Page 1
Page 1