Delineation of Ehlers–Danlos syndrome phenotype due to the c.934C>T, p.(Arg312Cys) mutation in <i>COL1A1</i>: Report on a three‐generation family without cardiovascular events, and literature review
Marina Colombi(University of Brescia), Marco Ritelli(University of Brescia), Arianna Zanca(Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia), Marina Venturini(University of Brescia), Piergiacomo Calzavara‐Pinton(University of Brescia), Chiara Dordoni(Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia)
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