C. Rime

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.

Y. Agid, J. Melki, A. Dürr, 1994, Human molecular genetics.

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families

J. Weissenbach, N. Baumann, A. Elbaz, 1994, Nature Genetics.

Mutations in the Muscle Sodium Channel Gene (SCN4A) in 13 French Families with Hyperkalemic Periodic Paralysis and Paramyotonia Congenita: Phenotype to Genotype Correlations and Demonstration of the Predominance of Two Mutations

G. Serratrice, F. Chapon, C. Confavreux, 1994, European journal of human genetics : EJHG.

Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia

J. Weissenbach, Y. Agid, N. Baumann, 1995, Neuromuscular Disorders.