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institution:"IIEPAE"
dc.subject.por.fl_str_mv:"Point mutation"
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Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome
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Petroni,Roberta Cardoso
Publication Date 2017
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Institution: IIEPAE
Subject: Point mutation
Institution
IIEPAE
Source
1
Einstein (São Paulo)
Author
1
Campregher,Paulo Vidal
1
Carvalho,Flavia Pereira de
1
Hamerschlak,Nelson
1
Hyppolito,Joyce Esteves
1
Nascimento,Claudia Mac Donald Bley
1
Petroni,Roberta Cardoso
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Rosa,Susana Elaine Alves da
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Santana,Rúbia Anita Ferraz
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Document type
1
Report
Language
1
eng
Subject
1
Case reports
1
Cataract
1
Ferritins
1
Genetics
1
Heredity
Point mutation
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