The neonatal progeroid syndrome (Wiedemann-Rautenstrauch): A model for the study of human aging?

Experimental Gerontology

Volumn 42, Issue 10, 2007, Pages 939-943

  Arboleda, Gonzalo ^a,b   Ramírez, Nelson ^a   Arboleda, Humberto ^a,c  

^a UNIVERSIDAD NACIONAL DE COLOMBIA   (Colombia)

^b UNIVERSIDAD NACIONAL DE COLOMBIA   (Colombia)

^c Facultad de Medicina   (Colombia)

Author keywords

Aging; AKT; Hutchinson Gilford progeria; Lamin A; Neonatal progeria; Wiedemann Rautenstrauch

Indexed keywords

INSULIN; LAMIN A; PROTEIN KINASE B;

AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL FEATURE; DENTITION; FACIES; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; HYPERCHOLESTEROLEMIA; HYPERINSULINISM; HYPERTRIGLYCERIDEMIA; LIPID STORAGE; PATHOPHYSIOLOGY; PREMATURE AGING; PRIORITY JOURNAL; PROGERIA; PROTEIN METABOLISM; SHORT STATURE; SHORT SURVEY; TELOMERE; WIEDEMANN RAUTENSTRAUCH SYNDROME; ZMPSTE24 GENE;

AGING; AGING, PREMATURE; HUMANS; INFANT, NEWBORN; LAMIN TYPE A; MODELS, BIOLOGICAL; MUTATION; PROGERIA; SYNDROME;

EID: 34548670496     PISSN: 05315565     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.exger.2007.07.004     Document Type: Short Survey

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