Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome.
Gene
; 529(1): 45-9, 2013 Oct 15.
Article
en En
| MEDLINE
| ID: mdl-23954227
Palabras clave
3D; A; ABI; Adenine; Applied Biosystems; C; Cys; Cysteine; Cytosine; DNA; Degree Celsius; Deoxyribose Nucleic Acid; Duplication; Exo-SAP; Exonuclease-Shrimp Alcaline Phosphatase; Frameshift; G; Guanine; KCl; Kb; Kilobase; Leu; Leucine; Ligand-binding sites prediction; Lys; Lysine; MIM; Magnesium chloride; Mendelian Inheritance in Man; MgCl2; Microliter; Micromole per liter; Millimolar; Neonatal diagnosis; Novel mutation; PCR; Picomole; Polymerase Chain Reaction; Potassium Chloride; Pro; Proline; Protein; RichnerHanhart syndrome; Second; T; Taq; Thermus aquaticus; Three-dimensional; Thymine; Tris(hydroxymethyl)aminomethane hydrochloride; TrisHCl; Trp; Tryptophan; Tunisian families; Tyr; Tyrosine; dup; fs; mM; p; pmol; s; µL; µmol/L
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Genes tat
/
Mutación Missense
/
Tirosinemias
Tipo de estudio:
Diagnostic_studies
/
Prognostic_studies
/
Screening_studies
Límite:
Child, preschool
/
Humans
/
Infant
/
Male
País/Región como asunto:
Africa
Idioma:
En
Revista:
Gene
Año:
2013
Tipo del documento:
Article
País de afiliación:
Túnez