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Author
Papendieck P
Papendieck P
References (2)
1. Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect - Bernal Barquero_2022_Int.J.Mol.Sci_23_9251
Title :
Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect -
Bernal Barquero_2022_Int.J.Mol.Sci_23_9251
Author(s) :
Bernal Barquero CE
,
Geysels RC
,
Jacques V
,
Carro GH
,
Martin M
,
Peyret V
,
Abregu MC
,
Papendieck P
,
Masini-Repiso AM
,
Savagner F
,
Chiesa AE
,
Citterio CE
,
Nicola JP
Ref :
Int J Mol Sci ,
23
:9251 , 2022
Abstract :
View Abstract
PubMedSearch :
Bernal Barquero_2022_Int.J.Mol.Sci_23_9251
PubMedID
:
36012511
Gene_locus related to this paper:
human-TG
2. Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism - Siffo_2018_Mol.Cell.Endocrinol_473_1
Title :
Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism -
Siffo_2018_Mol.Cell.Endocrinol_473_1
Author(s) :
Siffo S
,
Adrover E
,
Citterio CE
,
Miras MB
,
Balbi VA
,
Chiesa A
,
Weill J
,
Sobrero G
,
Gonzalez VG
,
Papendieck P
,
Martinez EB
,
Gonzalez-Sarmiento R
,
Rivolta CM
,
Targovnik HM
Ref :
Mol Cell Endocrinol ,
473
:1 , 2018
Abstract :
View Abstract
PubMedSearch :
Siffo_2018_Mol.Cell.Endocrinol_473_1
PubMedID
:
29275168
Gene_locus related to this paper:
human-TG