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pro vyhledávání: '"Sarada Vani"'
Autor:
Chanchal Kumar, Sarada Vani, Namita Neelkanth Deshmukh, Sujith Omkaram, Rajeev Pothala, Sushma Poornima Bathina, Deepika Dodda
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background Hereditary transient neonatal hyperparathyroidism (TNHP) is a rare autosomal-recessive condition caused by variants in TRPV6 gene which encodes for a transient maternal–fetal calcium transport channel. This is characterized by i
Externí odkaz:
https://doaj.org/article/a852e4d4f6e14689a7d031897e619ad2