Characterization of a novel mutation in F8 gene causing severe haemophilia A by deletion mapping with STS markers

E-ISSN： 1365-2516|21|2|e136-e139

ISSN： 1351-8216

Source： HAEMOPHILIA, Vol.21, Iss.2, 2015-03, pp. : e136-e139

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

A Novel Mutation (2409delT) in Exon 14 of the Factor VIII Gene Causes Severe Haemophilia A

Human Heredity, Vol. 50, Iss. 4, 2000-04 ,pp. : 266-267

Karger

Access to resources Recommend Favorite

Mapping of STS markers obtained from oat resistance gene analog sequences

By Loarce Yolanda Sanz María Jesús Irigoyen María L. Fominaya Araceli Ferrer Esther

Genome, Vol. 52, Iss. 7, 2009-07 ,pp. : 608-619

NRC Research Press

Access to resources Recommend Favorite

A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period

PEDIATRIC BLOOD & CANCER (ELECTRONIC), Vol. 61, Iss. 4, 2014-04 ,pp. : 763-764

John Wiley & Sons Inc

Access to resources Recommend Favorite

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

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

John Wiley & Sons Inc

Access to resources Recommend Favorite

Unexpected Peripheral Markers of Thyroid Function in a Patient with a Novel Mutation of the MCT8 Thyroid Hormone Transporter Gene

Hormone Research in Paediatrics, Vol. 67, Iss. 1, 2006-09 ,pp. : 1-6

Karger

Access to resources Recommend Favorite