Mutational and Bioinformatics Analysis of the Nkx2.1 Gene in a Cohort of Iranian Pediatric Patients with Congenital Hypothyroidism (Ch)

AuthID
 P-00X-0PV
9
Author(s)
Heidari, MM
·
Manshadi, SAM
·
Eshghi, AR
·
Talebi, F
·
Khatami, M
·
Ordooei, M
·
Chamani, R
·
Ghasemi, F
Document Type
Article
Year published
2022
Published
in PHYSIOLOGY INTERNATIONAL, ISSN: 2498-602X
Volume: 109, Issue: 2, Pages: 261-277 (17)
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Publication Identifiers
Pubmed: 35895569
SCOPUS: 2-s2.0-85135382575
Wos: WOS:000832211000010
Source Identifiers
ISSN: 2498-602X
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