Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism-Reference-Cited by-同舟云学术

Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism

Published:2020-09-15 Issue:10 Volume:47 Page:7467-7475
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Kollati Yedukondalu,Akella Radha Rama Devi,Naushad Shaik Mohammad,Borkar Divya,Thalla Maunika,Nagalingam Swapna,Lingappa Lokesh,Patel Rajesh K.,Reddy G. Bhanuprakash,Dirisala Vijaya R.^ORCID

Funder

DST-SERB

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s11033-020-05803-x.pdf

Reference25 articles.

1. Kaur G, Thakur K, Kataria S, Singh TR, Chavan BS, Kaur G, Atwal R (2016) Current and future perspective of newborn screening: an Indian scenario. J Pediatr Endocrinol Metab 29:5–13

2. Bhatia R, Rajwaniya D (2018) Congenital hypothyroidism screening in term neonates using umbilical cord blood TSH values. Indian J Endocrinol Metab 22:277–279

3. Christopher R, Radha Rama Devi A, Kabra M, Kapoor S, Mathur R, Muranjan M, Nigam PK, Pandey RM, Singh A, Suresh S (2018) ICMR Task Force on Inherited Metabolic Disorders. Newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia. Indian J Pediatr 85:935–940

4. Rastogi MV, LaFranchi SH (2010) Congenital hypothyroidism. Orphanet J Rare Dis 5:17

5. Long W, Zhou L, Wang Y, Liu J, Wang H, Yu B (2020) Complicated relationship between genetic mutations and phenotypic characteristics in transient and permanent congenital hypothyroidism: analysis of pooled literature data. Int J Endocrinol 2020:6808517

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