Digenic inheritance in medical genetics
Digenic inheritance (DI) is the simplest form of inheritance for genetically complex diseases. By contrast with the thousands of reports that mutations in single genes cause human diseases, there are only dozens of human disease phenotypes with evidence for DI in some pedigrees. The advent of high-t...
Main Author: | Schäffer, Alejandro A |
---|---|
Format: | Online |
Language: | English |
Published: |
BMJ Publishing Group
2013
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778050/ |
Similar Items
-
Digenic Inheritance in Cystinuria Mouse Model
by: Espino, Meritxell, et al.
Published: (2015) -
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
by: Konstantinos Voskarides, et al.
Published: (2018-05-01) -
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
by: Isabelle Schrauwen, et al.
Published: (2018-07-01) -
DIDA: A curated and annotated digenic diseases database
by: Gazzo, Andrea M., et al.
Published: (2016) -
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy
by: Esposito, Teresa, et al.
Published: (2013)