NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
| author | |
| created | [InstanceEdit:5336462] Jassal, Bijay, 2014-03-03 |
| dbId | 5336431 |
| displayName | NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter |
| journal | J. Biol. Chem. |
| pages | 8060-8 |
| pubMedIdentifier | 17166836 |
| schemaClass | LiteratureReference |
| title | NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter |
| url | http://www.ncbi.nlm.nih.gov/pubmed/17166836 |
| volume | 282 |
| year | 2007 |
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