Perin, Francesca

Two Novel Cases of Autosomal Recessive Noonan Syndrome Associated With LZTR1 Variants. [electronic resource] - Revista espanola de cardiologia (English ed.) Nov 2019 - 978-980 p. digital

Publication Type: Case Reports; Journal Article

1885-5857

10.1016/j.rec.2019.05.002 doi


Electrocardiography
Humans
Infant, Newborn
Male
Mutation
Noonan Syndrome--diagnosis
Pedigree
Phenotype
Transcription Factors--genetics