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Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders.
Endocr Connect. 2023 Jul 5;12(8):e220473. doi: 10.1530/EC-22-0473.
Endocr Connect. 2023.
PMID: 37166408
Free PMC article.
Cushing disease due to a somatic USP8 mutation in a patient with evolving pituitary hormone deficiencies due to a germline GH1 splicing variant.
Labello JH, Benedetti AFF, Azevedo BV, de Lima Jorge AA, Cescato VAS, Rosemberg S, Frasseto FP, Arnhold IJP, de Carvalho LRS.
Labello JH, et al.
Arch Endocrinol Metab. 2022 Mar 8;66(1):104-111. doi: 10.20945/2359-3997000000428. Epub 2022 Jan 13.
Arch Endocrinol Metab. 2022.
PMID: 35029852
Free PMC article.
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