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Autor:
Abdulla Shahid, BS, Naman S. Shetty, MD, Nirav Patel, MD, MSPH, Taylor McClinchey, MS, Garima Arora, MD, Pankaj Arora, MD
Publikováno v:
JACC: Case Reports, Vol 29, Iss 11, Pp 102343- (2024)
Phosphodiesterase 3A (PDE3A) gene mutations have recently been associated with hypertension and brachydactyly syndrome (HTNB). This report shows how the recent recognition of the role of the PDE3A gene in HTNB facilitated the diagnosis of HTNB in a 2
Externí odkaz:
https://doaj.org/article/15ed65dbc3204745b000bc81d8985d8d