Relapsing Pancreatitis due to a Novel Compound Heterozygosity in the CFTR Gene Involving the Second Most Common Mutation in Central and Eastern Europe [CFTRdele2,3(21 kb)]

Publisher： Karger

E-ISSN： 1424-3911|5|1|92-96

ISSN： 1424-3903

Source： Pancreatology, Vol.5, Iss.1, 2005-04, pp. : 92-96

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Bernard-Soulier Syndrome due to Compound Heterozygosity for a Novel Glycoprotein Ibβ Mutation

By  

Acta Haematologica, Vol. 131, Iss. 1, 2013-09 ,pp. : 46-49

Karger

Access to resources Recommend Favorite

CFTR Gene Mutation in Patients with Apparently Idiopathic Pancreatitis: Lack of Phenotype-Genotype Correlation

By  

Pancreatology, Vol. 10, Iss. 2-3, 2010-05 ,pp. : 158-164

Karger

Access to resources Recommend Favorite

Oguchi disease due to a novel mutation in the GRK1 gene

By  

ACTA OPHTHALMOLOGICA, Vol. 94, Iss. S256, 2016-10 ,pp. : n/a-n/a

John Wiley & Sons Inc

Access to resources Recommend Favorite

A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family

By Wei Qinjun   Liu Youguo   Wang Shuai   Liu Tingting   Lu Yajie   Xing Guangqian   Cao Xin  

International Journal of Molecular Medicine, Vol. 33, Iss. 2, 2014-02 ,pp. : 310-316

Spandidos Publications

Access to resources Recommend Favorite

A novel compound heterozygous mutation in the F13A gene causing hereditary factor XIII deficiency in a Chinese family

By  

JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol. 4, Iss. 1, 2006-01 ,pp. : 267-269

John Wiley & Sons Inc

Access to resources Recommend Favorite