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A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans.
Tuhan H, Ceylaner S, Nalbantoğlu Ö, Acar S, Abacı A, Böber E, Demir K. Tuhan H, et al. Among authors: acar s. J Clin Res Pediatr Endocrinol. 2017 Dec 15;9(4):371-374. doi: 10.4274/jcrpe.4577. Epub 2017 Jun 30. J Clin Res Pediatr Endocrinol. 2017. PMID: 28663160 Free PMC article.
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3.
Acar S, BinEssa HA, Demir K, Al-Rijjal RA, Zou M, Çatli G, Anık A, Al-Enezi AF, Özışık S, Al-Faham MSA, Abacı A, Dündar B, Kattan WE, Alsagob M, Kavukçu S, Tamimi HE, Meyer BF, Böber E, Shi Y. Acar S, et al. PLoS One. 2018 Mar 5;13(3):e0193388. doi: 10.1371/journal.pone.0193388. eCollection 2018. PLoS One. 2018. PMID: 29505567 Free PMC article.
281 results