Titolo | Pubblicato in | Anno |
---|---|---|
Protracted late infantile ceroid lipofuscinosis due to TPP1 mutations. clinical, molecular and biochemical characterization in three sibs | JOURNAL OF THE NEUROLOGICAL SCIENCES | 2015 |
Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathy. | GENE | 2015 |
Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome | NATURE GENETICS | 2015 |
The emerging role of MicroRNA in schizophrenia | CNS & NEUROLOGICAL DISORDERS. DRUG TARGETS | 2015 |
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