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URL: http://www.hemobase.com/en/Base_de_datos_HB.htm
Proper Citation: Haemophilia B Mutation Database (RRID:SCR_007699)
Description: It is a database of point mutations and short additions and deletions in the factor IX gene. The database attempts to offer a view of the spectrum of mutations causing haemophilia B that is as accurate as possible and this is helped by the fact that about 1/3 of all mutations have been detected as a result of full population studies. However, some bias cannot be completely avoided. Obviously there is an over-representation of severe haemophilia-causing mutations as these tend to be the first analysed and the most likely to come to notice. We also expect under-representation of double mutants as not all laboratories have done complete gene screens. Haemophilia B, Haemophilia B Mutation, IX, IX gene, IX gene mutation
Abbreviations: Haemophilia B Mutation Database
Synonyms: The Haemophilia B Mutation Database
Resource Type: data or information resource, database
Keywords: haemophilia b, haemophilia b mutation, ix, ix gene, ix gene mutation
Resource Name: Haemophilia B Mutation Database
Resource ID: SCR_007699
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
