NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter (Q28588664)
Jump to navigation
Jump to search
scientific journal article
Language | Label | Description | Also known as |
---|---|---|---|
English | NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter |
scientific journal article |
Statements
2 references
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter (English)
2 references
Angela Goytain
2 references
Alaa El-Husseini
2 references
2 references
282
2 references
11
2 references
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
2 references
2 references