Polymorphism of transglutaminase 2: unusually low frequency of genomic variants with deficient functions

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

The 2011 Nucleic Acids Research Database Issue and the online Molecular Biology Database Collection

(2010) M. Y. Galperin et al.   NUCLEIC ACIDS RESEARCH

Factor XIII and Atherothrombotic Diseases

(2010) László Muszbek et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

The TGM2 gene is associated with schizophrenia in a British population

(2009) Matilda Bradford et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Functional significance of five noncanonical Ca2+-binding sites of human transglutaminase 2 characterized by site-directed mutagenesis

(2009) Róbert Király et al.   FEBS Journal

A Missense Mutation in TGM5 Causes Acral Peeling Skin Syndrome in a Tunisian Family

(2009) Monia Kharfi et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery disease

(2009) Ahmet Var et al.   MOLECULAR BIOLOGY REPORTS

Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

(2009) R. Drmanac et al.   SCIENCE

Factor XIII Deficiency

(2009) Mehran Karimi et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS