Publication | Closed Access
A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy
11
Citations
24
References
2017
Year
Rare DiseasesDevelopmental BiologyNew Pla2g6 MutationInfantile Neuroaxonal DystrophyGenetic DisorderMendelian DisorderGeneticsDegenerative DiseaseAbnormal DevelopmentNeuropathologyMedicineNeurogenetics
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