Genotype/phenotype correlations in familial hypercholesterolaemia


Autoria(s): Nicholls, P.; Young, I.S.; Graham, C.A.
Data(s)

01/01/1998

Resumo

It is now possible to identify the specific gene defect in the majority of patients with familial hypercholesterolaemia. A potential benefit of this knowledge, in addition to helping with family screens, is to be able to predict the future clinical course. In order to do this, detailed genotype/phenotype correlation studies are required.

Identificador

http://pure.qub.ac.uk/portal/en/publications/genotypephenotype-correlations-in-familial-hypercholesterolaemia(d1a79e03-5de4-4283-8b05-541c89c20b19).html

http://dx.doi.org/10.1097/00041433-199808000-00005

http://www.scopus.com/inward/record.url?partnerID=yv4JPVwI&eid=2-s2.0-0031666905&md5=38d2c7ff98b205e4a0326aedbd39cb3e

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Nicholls , P , Young , I S & Graham , C A 1998 , ' Genotype/phenotype correlations in familial hypercholesterolaemia ' Current Opinion in Lipidology , vol 9 , no. 4 , pp. 313-317 . DOI: 10.1097/00041433-199808000-00005

Tipo

article