Prenatal diagnosis of respiratory chain deficiency by direct mutation screening-Reference-Cited by-同舟云学术

Prenatal diagnosis of respiratory chain deficiency by direct mutation screening

Published:2001-07 Issue:7 Volume:21 Page:602-604
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Amiel Jeanne,Gigarel Nadine,Benacki Alexandra,Benit Paule,Valnot Isabelle,Parfait Béatrice,Von Kleist-Retzow Jurgen-Christoph,Raclin Valérie,Hadj-Rabia Smaïl,Dumez Yves,Rustin Pierre,Bonnefont Jean-Paul,Munnich Arnold,Rötig Agnès

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference12 articles.

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2. Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency;Faivre;Prenat Diagn,2000

3. Molecular genetic aspects of human mitochondrial disorders;Larsson;Annu Rev Genet,1995

4. Mitochondrial respiratory chain disorders I: mitochondrial DNA defects;Leonard;Lancet,2000a

5. Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects;Leonard;Lancet,2000b

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