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Cited by in F6Publishing
For: D'Apice MR, De Dominicis A, Murdocca M, Amati F, Botta A, Sangiuolo F, Lattanzi G, Federici M, Novelli G. Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome. Acta Myol 2020;39:320-35. [PMID: 33458588 DOI: 10.36185/2532-1900-036] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
Number Citing Articles
1 Ferradini V, Cosma J, Romeo F, De Masi C, Murdocca M, Spitalieri P, Mannucci S, Parlapiano G, Di Lorenzo F, Martino A, Fedele F, Calò L, Novelli G, Sangiuolo F, Mango R. Clinical Features of LMNA-Related Cardiomyopathy in 18 Patients and Characterization of Two Novel Variants. J Clin Med 2021;10:5075. [PMID: 34768595 DOI: 10.3390/jcm10215075] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]