Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALS.

BACKGROUND: The homogeneous genotype and stereotyped phenotype of a unique familial form of amyotrophic lateral sclerosis (ALS) (patients homozygous for aspartate-to-alanine mutations in codon 90 (homD90A) superoxide dismutase 1) provides an ideal model for studying genotype/phenotype interactions a...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Blain, C, Brunton, S, Williams, VC, Leemans, A, Turner, MR, Andersen, P, Catani, M, Stanton, B, Ganesalingham, J, Jones, D, Williams, S, Leigh, P, Simmons, A
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	2011

Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALS ανά Blain, C, Brunton, S, Williams, VC, Leemans, A, Turner, M, Andersen, P, Catani, M, Stanton, B, Ganesalingham, J, Jones, D, Williams, S, Leigh, P, Simmons, A

Έκδοση 2011

Journal article

Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALS.

Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALS ανά Blain, C, Brunton, S, Williams, VC, Leemans, A, Turner, M, Andersen, P, Catani, M, Stanton, B, Ganesalingham, J, Jones, D, Williams, S, Leigh, P, Simmons, A

Παρόμοια τεκμήρια