H. Kobayashi

Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15

E. Hoffman, C. Mariani, E. Farina, 1999, Neurology.

A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2.

T C Matise, F Greenberg, T. Matise, 1995, Human molecular genetics.

Brief Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor- (cid:1) B activation: common genetic etiology with Blau syndrome

A. Utani, H. Tsutsumi, T. Nakahata, 2005 .

Familial Parkinson's disease. Alpha-synuclein and parkin.

S. Minoshima, N. Shimizu, N. Hattori, 2001, Advances in neurology.