Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family.
Abosabie SAS, Abosabie SA, Alfaifi J, Alqahtani YA, Shati AA, Alotaibi NA, Alghamdi OA, Alotaibi GN, Baabdullah AA, Kabrah LK, Kamal NM, Oshi MAM, Abdallah EAA.
Abosabie SAS, et al. Among authors: alqahtani ya.
Mol Genet Genomic Med. 2024 Jan;12(1):e2314. doi: 10.1002/mgg3.2314. Epub 2023 Nov 8.
Mol Genet Genomic Med. 2024.
PMID: 37937857
Free PMC article.
Review.