Alström syndrome caused by deletion in ALMS1 gene fixed in a Northern Pakistan recurrent haplotype (C. Monzó, F. G.-. Ferrer, J. C. F. García, A. Amadoz, D. Albuquerque, F. B. Angueira, G. Marcaida, & R. R.-. López, Trans.). (2020). Indian Journal of Case Reports, 3(4), 171-174. https://doi.org/10.32677/IJCR.2017.v03.i04.001