SMRT Compounds Correct Nonsense Mutations in Primary Immunodeficiency and Other Genetic Models

Annals of the New York Academy of Sciences - United States
doi 10.1111/j.1749-6632.2012.06467.x
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Activating PI3Kδ Mutations in a Cohort of 669 Patients With Primary Immunodeficiency

Clinical and Experimental Immunology
AllergyImmunology
2015English

X-Linked Primary Immunodeficiency Associated With Hemizygous Mutations in the Moesin (MSN) Gene

Journal of Allergy and Clinical Immunology
AllergyImmunology
2016English

Genetic Paradox Explained by Nonsense

Nature
Multidisciplinary
2019English

Correction To: Use of Genetic Testing for Primary Immunodeficiency Patients

Journal of Clinical Immunology
AllergyImmunology
2018English

Primary Immunodeficiency: Common Variable Immunodeficiency

Journal of Clinical Medicine of Kazakhstan
2016English

SF3B1 Mutations in Primary Myelofibrosis: Clinical, Histopathology and Genetic Correlates Among 155 Patients

Leukemia
Cancer ResearchOncologyAnesthesiologyPain MedicineHematology
2011English

Current Genetic Models for Prediction of Primary Myelofibrosis

Klinicheskaya Onkogematologiya/Clinical Oncohematology
OncologyHematology
2019English

Diophantine Correct Models of Arithmetic

Proceedings of the American Mathematical Society
MathematicsApplied Mathematics
1979English

Primary Immunodeficiency Diseases.

Annals of Internal Medicine
Internal MedicineMedicine
1984English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy