Alström syndrome caused by deletion in ALMS1 gene fixed in a Northern Pakistan recurrent haplotype. Indian Journal of Case Reports, [S. l.], v. 3, n. 4, p. 171–174, 2020. DOI: 10.32677/IJCR.2017.v03.i04.001. Disponível em: https://mansapublishers.com/index.php/ijcr/article/view/403.. Acesso em: 24 nov. 2024.