论文信息 - Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function - 字舞流文

Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function

A. Singleton | B. Wirth | A. Durr | A. Brice | G. Stevanin | S. Zuchner | M. Riessland | M. Coutelier | M. Hammerschmidt | M. Karakaya | Seyyedmohsen Hosseinibarkooie | Heiko Löhr | E. Janzen | C. Pichlo | Natalia Mendoza-Ferreira | S. Schneider | Laura Torres-Benito | J. Milbradt | Marie Coutelier