Author

Mich�le Schmitt

Observed institutions: Centre National de la Recherche Scientifique, Inserm, Institut de génétique et de biologie moléculaire et cellulaire, Hôpitaux Universitaires de Strasbourg

OpenAlex ID: A5110021602

Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

1999 · Mireille Coss�e, Alexandra D�rr, et al. · Annals of Neurology · 389

Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome

2001 · Jean-Pierre Delaunoy, Fatima Abidi, et al. · Human Mutation · 91

Works count: 2

Citation count: 480

H-index: 2

I10-index: 2