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Novel mitochondrial DNA mutations implicated in Noonan syndrome

✍ Scribed by Perundurai S. Dhandapany; Sakthivel Sadayappan; Ayyasamy Vanniarajan; Bose Karthikeyan; Chandran Nagaraj; Kalpana Gowrishankar; Govindan Sadasivam Selvam; Lalji Singh; Kumarasamy Thangaraj

Book ID
116545199
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
259 KB
Volume
120
Category
Article
ISSN
0167-5273

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## Abstract Noonan syndrome (NS) is the most common non‐chromosomal syndrome seen in children and is characterized by short stature, dysmorphic facial features, chest deformity, a wide range of congenital heart defects and developmental delay of variable degree. Mutations in the Ras/mitogen‐activat