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NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
- Source :
- Clinical Genetics
- Publication Year :
- 2021
- Publisher :
- Blackwell Publishing Ltd, 2021.
- Subjects :
- Adult
Male
Thyroid Nuclear Factor 1
Bioinformatics
Text mining
Chorea
Cell Line, Tumor
Brain-Lung-Thyroid Syndrome
Genetics
Congenital Hypothyroidism
Medicine
Humans
Amino Acid Sequence
Letters to the Editor
Child
Letter to the Editor
Athetosis
Genetics (clinical)
Aged
Respiratory Distress Syndrome, Newborn
business.industry
Middle Aged
Mutation (genetic algorithm)
Mutation
Female
business
HeLa Cells
Subjects
Details
- Language :
- English
- ISSN :
- 13990004 and 00099163
- Volume :
- 100
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Clinical Genetics
- Accession number :
- edsair.doi.dedup.....c2be1f8e3cd79b697ff1546ec475db93