Identification of a Novel Frame-Shift Mutation in PRSS1 Gene in Han Patients with Autoimmune Pancreatitis

By  

Current Molecular Medicine, Vol. 14, Iss. 3, 2014-03 ,pp. : 340-348

Bentham Science Publishers

Access to resources Recommend Favorite

Gene Conversion-like Missense Mutations in the Human Cationic Trypsinogen Gene and Insights into the Molecular Evolution of the Human Trypsinogen Family

By Chen J-M.   Ferec C.  

Molecular Genetics and Metabolism, Vol. 71, Iss. 3, 2000-11 ,pp. : 463-469

Academic Press

Access to resources Recommend Favorite

Two Novel Missense Mutations of the HFE Gene (I105T and G93R) and Identification of the S65C Mutation in Alabama Hemochromatosis Probands

By Barton J.C.   Sawada-Hirai R.   Rothenberg B.E.   Acton R.T.  

Blood Cells, Molecules, and Diseases, Vol. 25, Iss. 3, 1999-06 ,pp. : 147-155

Academic Press

Access to resources Recommend Favorite

A Novel Missense Mutation in Human Lactate Dehydrogenase B-Subunit Gene

By Takatani T.   Takaoka N.   Tatsumi M.   Kawamoto H.   Okuno Y.   Morita K.   Masutani T.   Murakawa K.   Okamoto Y.  

Molecular Genetics and Metabolism, Vol. 73, Iss. 4, 2001-08 ,pp. : 344-348

Academic Press

Access to resources Recommend Favorite

Spectrum of mutations in the arylsulfatase A gene in a Canadian DNA collection including two novel frameshift mutations, a new missense mutation (C488R) and an MLD mutation (R84Q) in cis with a pseudodeficiency allele

By Coulter-Mackie M.B.   Gagnier L.  

Molecular Genetics and Metabolism, Vol. 79, Iss. 2, 2003-06 ,pp. : 91-98

Elsevier

Access to resources Recommend Favorite