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  4. Identification of a new mutation in RSK2, the gene for coffin¿lowry syndrome (CLS), in two related patients with mild and atypical phenotypes
 
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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)
Di Stazio Mariateresa 
Bigoni Stefania
Iuso Nicola
Vuch Josef
Selvatici Rita
Ulivi Sheila 
D'Adamo Adamo Pio 
DOI
10.3390/BRAINSCI11081105
Project(s)
Identificazione di fattori genetici e ambientali associati a tratti complessi in popolazioni isolate 
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C.A.R.S.O. - I.R.C.C.S. materno infantile Burlo Garofolo

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