Mild phenotype in two siblings with a missense GHR variant.
Sarıkaya Özdemir B, Çetinkaya S, Güleray Lafcı N, Şakar M, Karacan Küçükali G, Elmaoğullari S, Savaş Erdeve Ş.
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J Pediatr Endocrinol Metab. 2021 Jul 1;34(10):1349-1354. doi: 10.1515/jpem-2021-0044. Print 2021 Oct 26.
J Pediatr Endocrinol Metab. 2021.
PMID: 34218547