Suchergebnisse - "Ferradini, Valentina"

PubPharm (4)

1

Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome : A 10-year single center experience

enthalten in: Clinica chimica acta; international journal of clinical chemistry | 2020

von Mannucci, L. | Luciano, S. | Salehi, L. | +9

2

Targeted Next Generation Sequencing in patients with Myotonia Congenita

enthalten in: Clinica chimica acta; international journal of clinical chemistry | 2017

von Ferradini, V. | Cassone, M. | Nuovo, S. | +5

3

Genotype-phenotype correlation of F484L mutation in three Italian families with Thomsen myotonia

enthalten in: Muscle & nerve | 2017

von Cassone, M. | Ferradini, V. | Longo, G. | +7

4

Genotype–phenotype correlation of F484L mutation in three Italian families with Thomsen myotonia

enthalten in: Muscle & nerve | 2017

von Cassone, M. | Ferradini, V. | Longo, G. | +7

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