A novel case of homozygous LDLRAP1 gene mutation causing autosomal recessive familial hypercholesterolemia in Kuwait

Journal article

Peer reviewed

K.F.M.F. Alelaj, N.I. Alrajhi, A.J. Alsarraf and M.A. Aljarallah

Atherosclerosis, Vol.315, pp.e221-e221

12/2020

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Title: A novel case of homozygous LDLRAP1 gene mutation causing autosomal recessive familial hypercholesterolemia in Kuwait
Creators - without role: K.F.M.F. Alelaj - Ministry of Health
N.I. Alrajhi - Ministry of Health
A.J. Alsarraf - Ministry of Health
M.A. Aljarallah
Publication Details: Atherosclerosis, Vol.315, pp.e221-e221
Identifiers: 9916606108331
Academic Unit: Imam Mohammad Ibn Saud Islamic University (IMSIU)
Language: English
Resource Type: Journal article