Ontology highlight
ABSTRACT:
SUBMITTER: Ma L
PROVIDER: S-EPMC7586877 | biostudies-literature | 2020 Nov
REPOSITORIES: biostudies-literature
Ma Liyan L Tian Yu Y Peng Chenxing C Zhang Yiran Y Zhang Songyun S
Intractable & rare diseases research 20201101 4
Acute intermittent porphyria (AIP) is a dominant inherited disorder with a low penetrance that is caused by mutations in the gene coding for hydroxymethylbilane synthase (HMBS). Information about the epidemiology and molecular genetic features of this rare disorder is crucial to clinical research, and particularly to the evaluation of new treatments. Variations in the prevalence and penetrance of AIP in various studies may due to the different inclusion criteria and methods of assessment. Here, ...[more]