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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