Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification (2013)
Hsu, Sandy Chan; Sears, Renee L.; Lemos, Roberta R.; Zatz, Mayana 
Source: Neurogenetics. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA
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HSU, Sandy Chan et al. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification. Neurogenetics, v. 14, p. online, 2013Tradução . . Disponível em: https://doi.org/10.1007/s10048-012-0349-2. Acesso em: 11 nov. 2024.APA
Hsu, S. C., Sears, R. L., Lemos, R. R., & Zatz, M. (2013). Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification. Neurogenetics, 14, online. doi:10.1007/s10048-012-0349-2NLM
Hsu SC, Sears RL, Lemos RR, Zatz M. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification [Internet]. Neurogenetics. 2013 ; 14 online.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10048-012-0349-2Vancouver
Hsu SC, Sears RL, Lemos RR, Zatz M. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification [Internet]. Neurogenetics. 2013 ; 14 online.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10048-012-0349-2
