Cystic Fibrosis Resources
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GDB CFTR entry
"GDB's mission is to make available to scientists an encyclopedia of the human genome that is being constantly
revised and updated to reflect the current state of scientific knowledge."
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Cystic Fibrosis Resource Center
"This site has been produced by Solvay Healthcare Ltd., and is designed to be a useful source of information for cystic fibrosis patients, parents, doctors and other carers. Resources are provided which will hopefully help you in resolving problems and coping better with cystic fibrosis on a daily basis."
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Online Mendelian Inheritance in Man CFTR entry
"This database is a catalog of human genes and genetic
disorders authored and edited by Dr. Victor A. McKusick and his colleagues at Johns Hopkins and elsewhere, and
developed for the World Wide Web by NCBI, the National Center for Biotechnology Information. The database
contains textual information, pictures, and reference information. It also contains copious links to NCBI's Entrez
database of MEDLINE articles and sequence information."
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Canadian CF Foundation
Canadian CF Foundation
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Cystic Fibrosis Research, Inc.
Cystic Fibrosis Research, Inc.'s mission is to fund cystic fibrosis research and to offer educational and support programs
in a safe and healthy environment. Founded in 1975 as an independent nonprofit organization, CFRI is dedicated to
improving, extending and saving the lives of children and adults who have cystic fibrosis.
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Cystic-L Cystic Fibrosis Information & Support
"CYSTIC-L is a free email service dedicated to the exchange of information and support specific to cystic fibrosis."
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NIH Consensus Development Statement re: Genetic Testing for Cystic Fibrosis
"NIH Consensus Statements are prepared by a nonadvocate, non-Federal panel of experts, based on (1) presentations by investigators working in areas relevant to the consensus questions during a 2-day public session; (2) questions and statements from conference attendees during open discussion periods that are part of the public session; and (3) closed deliberations by the panel during the remainder of the second day and morning of the third."
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CF-WEB
"A growing collection of on-line information about Cystic Fibrosis. The primary focus will be collecting
and indexing existing support information and making it available to the CF community--people with Cystic
Fibrosis and their parents, friends and family--via the Internet."
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European Thematic Network for Cystic Fibrosis
The Thematic Network on CF creates a unique platform for scientists involved in fundamental CF research, for the
more than 160 genetic diagnostic laboratories, for CF associations of families, patients and clinicians, ethical, legal and IPR experts and representatives of the industry.
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Cystic Fibrosis Infomation from Norma Kennedy Plourde
This website is run by Norma Kennedy Plourde (RN) from Baker Lake, New Brunswick, Canada, who is also CF patient. Norma runs her website to educate and inform public about cystic fibrosis. A lot of useful information! Please visit Norma's website.
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Cystic Fibrosis MD
An educational site dedicated to keep you informed of cystic fibrosis issues.
Other Mutation Databases
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BTKbase
Mutation database for X-linked agammaglobulinemia.
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