CrossRef Text and Data Mining
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Rare PTH Gene Mutations Causing Parathyroid Disorders: A Review
Joon-Hyop Lee, Munkhtugs Davaatseren, Sihoon Lee
Endocrinol Metab. 2020;35(1):64-70.   Published online March 19, 2020
DOI: https://doi.org/10.3803/EnM.2020.35.1.64

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Abnormal dentin structure in two novel gene mutations [COL1A1, Arg134Cys] and [ADAMTS2, Trp795-to-ter] causing rare type I collagen disorders
Archives of Oral Biology. 2007;52(2):101-109   Crossref logo
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Novel compound heterozygous mutations in PLEC gene causing epidermolysis bullosa simplex with muscular dystrophy, case series of two affected sisters
Neuromuscular Disorders. 2017;27:S112-S113   Crossref logo
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RarePTHGene Mutations Causing Parathyroid Disorders: A Review
Endocrinology and Metabolism. 2020;35(1):64   Crossref logo
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G.P.3.03 Recurrent mutations in the NDUFS2 gene causing isolated complex I deficiency in skeletal muscle
Neuromuscular Disorders. 2009;19(8-9):562   Crossref logo
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P.289Precise gene editing of LGMD2A causing mutations
Neuromuscular Disorders. 2019;29:S151   Crossref logo
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Characterization of the 3′ splicing pattern of parathyroid hormone-related peptide (PTH-rP) and the expression of the PTH-rP gene and the PTH/PTH-rP receptor gene in human lung cancer
Lung Cancer. 1994;11:24   Crossref logo
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Inactivating PTH/PTHrP Signaling Disorders
Frontiers of Hormone Research. 2018;147-159   Crossref logo
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Parathyroid Hormone (PTH) Suppresses Rat PTH/PTH-Related Protein Receptor Gene Promoter
Biochemical and Biophysical Research Communications. 2001;287(2):313-322   Crossref logo
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Mitochondrial DNA mutations in oxyphilic and chief cell parathyroid adenomas
BMC Endocrine Disorders. 2007;7(1):   Crossref logo
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One beginning, many ends: Mutations in one gene causing varied clinical entities
Movement Disorders. 2011;26(3):379-379   Crossref logo
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