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Cited by in CrossRef
For: Lin SZ, Ma QJ, Pang QM, Chen QD, Wang WQ, Li JY, Zhang SL. Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report. World J Clin Cases 2022; 10(31): 11486-11492 [PMID: 36387827 DOI: 10.12998/wjcc.v10.i31.11486]
URL: https://www.wjgnet.com/2307-8960/full/v10/i31/11486.htm
Number Citing Articles
1
Åsa Kjellgren, Elenor Lundgren, Irina Golovleva, Berit Kriström, Mimmi Werner. Hearing impairment and vestibular function in patients with a pathogenic splice variant in the LHX3 geneBMC Medical Genomics 2024; 17(1) doi: 10.1186/s12920-024-02049-5