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Volumn 62, Issue 3, 2004, Pages 149-155

Compound heterozygous and homozygous mutations of the TSHβ gene as a cause of congenital central hypothyroidism in Europe

Author keywords

Allele; Gene mutations; Hypothyroidism; Neonatal screening; TSH deficiency

Indexed keywords

THYROTROPIN BETA SUBUNIT;

EID: 4644297657     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000080071     Document Type: Article
Times cited : (35)

References (25)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.