pseudohypoparathyroidism

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1
Frequency of variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2.
Vado, Yerai;Pereda, Arrate;Manero-Azua, Africa;, ;Perez de Nanclares, Guiomar;
2022 Frontiers in endocrinology DOI: 1055431 83 views
2
Bidirectional disruption of transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B.
Iwasaki, Yorihiro; Reyes, Monica; Ryabets-Lienhard, Anna; Gales, Barbara; Linglart, Agnès; Miller, D...
2025 Proceedings of the National Academy of Sciences of... DOI: 10.1073/pnas.2423271... 15 views

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Frontiers in endocrinology
ISSN: 1664-2392 691 views

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