Identification of a new mutation in RSK2, the gene for coffin¿lowry syndrome (CLS), in two related patients with mild and atypical phenotypes

Journal
Brain Sciences
ISSN
2076-3425
Author(s)
Bigoni Stefania
Iuso Nicola
Vuch Josef
Selvatici Rita
DOI
10.3390/BRAINSCI11081105
Project(s)