Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by A Bouhouche
Mutation in the Epsilon Subunit of the Cytosolic Chaperonin-Containing T-Complex Peptide-1 (Cct5) Gene Causes Autosomal Recessive Mutilating Sensory Neuropathy With Spastic Paraplegia
Journal of Medical Genetics
Genetics
Related publications
Autosomal Recessive Spastic Paraplegia Type 14
Autosomal Recessive Spastic Paraplegia Type 44
Autosomal Recessive Spastic Paraplegia Type 70
Autosomal Recessive Spastic Paraplegia Type 55
Autosomal Recessive Spastic Paraplegia Type 45
Autosomal Recessive Spastic Paraplegia Type 67
Autosomal Recessive Spastic Paraplegia Type 11
Autosomal Recessive Spastic Paraplegia Type 24
Autosomal Recessive Spastic Paraplegia Type 77
