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Publications by M. I. New

Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2013English

RNAi-mediated Silencing of Hepatic Alas1 Effectively Prevents and Treats the Induced Acute Attacks in Acute Intermittent Porphyria Mice

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2014English

Mutations in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia and Hypertension Cluster in Exons 6, 7, and 8.

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
1993English

Two Genes Encoding Steroid 21-Hydroxylase Are Located Near the Genes Encoding the Fourth Component of Complement in Man.

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
1985English

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