The Sunday Papers (26 February '06 edition)
Waters et al.
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes
Greenway et al.
ANG mutations segregate with familial and ‘sporadic’ amyotrophic lateral sclerosis
Repping et al.
High mutation rates have driven extensive structural polymorphism among human Y chromosomes
Rohmann et al.
Mutations in different components of FGF signaling in LADD syndrome
Comments welcome.
