Advertisement

Browse Subject Areas

?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

Frameshift mutation

Genotype-Phenotype Correlations in a Mountain Population Community with High Prevalence of Wilson’s Disease: Genetic and Clinical Homogeneity

Relu Cocoş, Alina Şendroiu, [ ... ], Florina Raicu

Mutations in SACPD-C Result in a Range of Elevated Stearic Acid Concentration in Soybean Seed

Militza Carrero-Colón, Nathan Abshire, [ ... ], Karen Hudson

Characterization of a New CDC73 Missense Mutation that Impairs Parafibromin Expression and Nucleolar Localization

Giulia Masi, Maurizio Iacobone, [ ... ], Luisa Barzon

Population-Based Analysis of Invasive Nontypeable Pneumococci Reveals That Most Have Defective Capsule Synthesis Genes

In Ho Park, K. Aaron Geno, [ ... ], Bernard Beall

Novel and Recurrent MYO7A Mutations in Usher Syndrome Type 1 and Type 2

Weining Rong, Xue Chen, [ ... ], Chen Zhao

A Truncated Form of Rod Photoreceptor PDE6 β-Subunit Causes Autosomal Dominant Congenital Stationary Night Blindness by Interfering with the Inhibitory Activity of the γ-Subunit

Gaël Manes, Pallavi Cheguru, [ ... ], Philippe Brabet

Genetic Analysis of Genes Related to Tight Junction Function in the Korean Population with Non-Syndromic Hearing Loss

Min-A Kim, Ye-Ri Kim, [ ... ], Un-Kyung Kim

Deletion in the EVC2 Gene Causes Chondrodysplastic Dwarfism in Tyrolean Grey Cattle

Leonardo Murgiano, Vidhya Jagannathan, [ ... ], Cord Drögemüller

A High-Throughput Colorimetric Screening Assay for Terpene Synthase Activity Based on Substrate Consumption

Maiko Furubayashi, Mayu Ikezumi, [ ... ], Daisuke Umeno

Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese

Yi-Lei Wu, Daw-Yang Hwang, [ ... ], Yann-Jinn Lee

TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia

Tsutomu Ogata, Tetsuya Niihori, [ ... ], Yoichi Matsubara

Comprehensive Molecular Diagnosis of Bardet-Biedl Syndrome by High-Throughput Targeted Exome Sequencing

Dong-Jun Xing, Hong-Xing Zhang, [ ... ], Zi-Bing Jin

Comparative Genomic Analysis of Primary and Synchronous Metastatic Colorectal Cancers

Sun Young Lee, Farhan Haq, [ ... ], Won-Suk Lee

Advertisement

Create a weekly email alert for: Frameshift mutation

You can change these options by clicking profile then "Alerts and Notifications"