Homozygous Sequence Variants in theNPR2Gene Underlying Acromesomelic Dysplasia Maroteaux Type (AMDM) in Consanguineous Families

Identification and Functional Characterization of Two NovelNPR2Mutations in Japanese Patients With Short Stature

(2014) Naoko Amano et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene

(2013) Kohji Miura et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Natriuretic peptides in cardiovascular diseases: current use and perspectives

(2013) M. Volpe et al.   EUROPEAN HEART JOURNAL

An Activating Mutation in the Kinase Homology Domain of the Natriuretic Peptide Receptor-2 Causes Extremely Tall Stature Without Skeletal Deformities

(2013) Sabine E. Hannema et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature

(2013) Gabriela A. Vasques et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Novel mutations in natriuretic peptide receptor-2 gene underlie acromesomelic dysplasia, type maroteaux

(2012) Saadullah Khan et al.   BMC Medical Genetics

An Overgrowth Disorder Associated with Excessive Production of cGMP Due to a Gain-of-Function Mutation of the Natriuretic Peptide Receptor 2 Gene

(2012) Kohji Miura et al.   PLoS One

Nitric oxide, C-type natriuretic peptide and cGMP as regulators of endochondral ossification

(2008) Cristina C. Teixeira et al.   DEVELOPMENTAL BIOLOGY