Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms.

Journal of medical genetics

Volumn 41, Issue 6, 2004, Pages

  Cremonesi, L ^a   Cozzi, A ^a   Girelli, D ^a   Ferrari, F ^a   Fermo, I ^a   Foglieni, B ^a   Levi, S ^a   Bozzini, C ^a   Camparini, M ^a   Ferrari, M ^a   Arosio, P ^a  

^a SAN RAFFAELE HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

APOFERRITIN; FERRITIN;

ARTICLE; BLOOD; CASE REPORT; CATARACT; GENETICS; HEMATOLOGIC DISEASE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; METHODOLOGY; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; PATHOLOGY; POINT MUTATION; START CODON;

APOFERRITINS; BASE SEQUENCE; CATARACT; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CODON, INITIATOR; DNA MUTATIONAL ANALYSIS; FERRITINS; HEMATOLOGIC DISEASES; HUMANS; NERVOUS SYSTEM DISEASES; POINT MUTATION;

EID: 19444383339     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2003.011718     Document Type: Article

References (0)