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

E-ISSN： 1538-7836|4|1|267-269

ISSN： 1538-7933

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

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

Related content

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

Characterization of a Cys329Gly Mutation Causing Hereditary Factor VII Deficiency

Acta Haematologica, Vol. 116, Iss. 2, 2006-08 ,pp. : 96-100

Karger

Access to resources Recommend Favorite

Identification of two novel missense mutations causing severe factor XIII deficiency

HAEMOPHILIA, Vol. 21, Iss. 3, 2015-05 ,pp. : e253-e256

John Wiley & Sons Inc

Access to resources Recommend Favorite

A novel mutation of the fumarase gene in a family with autosomal recessive fumarase deficiency

By Remes Anne Filppula Sirpa Rantala Heikki Leisti Jaakko Ruokonen Aimo Sharma Satyan Juffer André Hiltunen J.

Journal of Molecular Medicine, Vol. 82, Iss. 8, 2004-08 ,pp. : 550-554

Springer Publishing Company

Access to resources Recommend Favorite

Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiency

HAEMOPHILIA, Vol. 21, Iss. 2, 2015-03 ,pp. : 241-248

John Wiley & Sons Inc

Access to resources Recommend Favorite