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Mutation databases

PMCA4 (ATP2B4) Mutation in Familial Spastic Paraplegia

Miaoxin Li, Philip Wing-Lok Ho, [ ... ], Shu-Leong Ho

Computational Screening and Molecular Dynamic Simulation of Breast Cancer Associated Deleterious Non-Synonymous Single Nucleotide Polymorphisms in TP53 Gene

Kumaraswamy Naidu Chitrala, Suneetha Yeguvapalli

IthaGenes: An Interactive Database for Haemoglobin Variations and Epidemiology

Petros Kountouris, Carsten W. Lederer, [ ... ], Marina Kleanthous

Meta-Analysis of EGFR Tyrosine Kinase Inhibitors Compared with Chemotherapy as Second-Line Treatment in Pretreated Advanced Non-Small Cell Lung Cancer

Ning Li, Lu Yang, [ ... ], Si-yu Wang

Reversion and T Cell Escape Mutations Compensate the Fitness Loss of a CD8⁺ T Cell Escape Mutant in Their Cognate Transmitted/Founder Virus

Hongshuo Song, Bhavna Hora, [ ... ], Feng Gao

Integrated Analysis of Mutation Data from Various Sources Identifies Key Genes and Signaling Pathways in Hepatocellular Carcinoma

Yuannv Zhang, Zhaoping Qiu, [ ... ], Lu Xie

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

Mireia Alcalde, Oscar Campuzano, [ ... ], Ramon Brugada

Moving Away from Ritonavir, Abacavir, Tenofovir, and Efavirenz (RATE) - Agents That Concern Prescribers and Patients: A Feasibility Study and Call for a Trial

Amit C. Achhra, Mark A. Boyd, [ ... ], David A. Cooper

Panel Based MALDI-TOF Tumour Profiling Is a Sensitive Method for Detecting Mutations in Clinical Non Small Cell Lung Cancer Tumour

James L. Sherwood, Susanne Müller, [ ... ], Jill Walker

HIV-1 Diversity and Drug-Resistant Mutations in Infected Individuals in Changchun, China

Ming Yan, Ke Zhao, [ ... ], Xiao-Fang Yu

Screening for Streptomycin Resistance-Conferring Mutations in Mycobacterium tuberculosis Clinical Isolates from Poland

Tomasz Jagielski, Helena Ignatowska, [ ... ], Jacek Bielecki

Exome Sequencing Identifies DLG1 as a Novel Gene for Potential Susceptibility to Crohn's Disease in a Chinese Family Study

Shufang Xu, Feng Zhou, [ ... ], Bing Xia

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

Zied Riahi, Crystel Bonnet, [ ... ], Christine Petit

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