Finding a very rare mutation in non-Caucasian LCAT patients from Southwest Asia for the first time.
Farshid OliaeiBehdokht BatebiReza TabaripourHaleh Akhavan NiakiPublished in: Journal of cellular biochemistry (2018)
In this study, a very rare variation was reported for the first time in this part of the world. Investigation of a larger number of LCAT patients in different parts of Iran can provide availability of mutations panel that is useful for phenotype prediction and also prenatal diagnosis programming in families with a previous history of the disease.