TY  - GEN
AU  - Aldahmesh,Mohamed A
AU  - Abu-Safieh,Leen
AU  - Khan,Arif O
AU  - Al-Hassnan,Zuhair N
AU  - Shaheen,Ranad
AU  - Rajab,Mohammed
AU  - Monies,Dorota
AU  - Meyer,Brian F
AU  - Alkuraya,Fowzan S
TI  - Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example
SN  - 1552-4833
PY  - 2009///0617
KW  - Alleles
KW  - Base Sequence
KW  - Cardiomyopathy, Dilated
KW  - genetics
KW  - Cell Cycle Proteins
KW  - Child
KW  - Child, Preschool
KW  - Codon, Nonsense
KW  - Consanguinity
KW  - DNA
KW  - DNA Mutational Analysis
KW  - Female
KW  - Frameshift Mutation
KW  - Hearing Loss, Sensorineural
KW  - Heterozygote
KW  - Homozygote
KW  - Humans
KW  - Insulin Resistance
KW  - Liver Failure
KW  - Male
KW  - Mutation
KW  - Obesity
KW  - Proteins
KW  - Renal Insufficiency
KW  - Retinitis Pigmentosa
KW  - Saudi Arabia
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.a.32753
ER  -