Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Gary A. Quamme
NIPA1(SPG6), the Basis for Autosomal Dominant Form of Hereditary Spastic Paraplegia, Encodes a Functional Mg2+Transporter
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Autosomal Dominant Hereditary Spastic Paraplegia: Novel Mutations in the REEP1 Gene (SPG31)
BMC Medical Genetics
Genetics
Autosomal Dominant Spastic Paraplegia Type 37
Autosomal Dominant Spastic Paraplegia Type 8
Autosomal Dominant Spastic Paraplegia Type 13
Autosomal Dominant Spastic Paraplegia Type 41
Autosomal Dominant Spastic Paraplegia Type 19
MR Imaging Findings in Autosomal Recessive Hereditary Spastic Paraplegia
American Journal of Neuroradiology
Medicine
Nuclear Medicine
Neurology
Imaging
Radiology
Hereditary Spastic Paraplegia
Schweizer Archiv für Neurologie und Psychiatrie
A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-Q34
American Journal of Human Genetics
Genetics
