Molecular Analysis and Prenatal Diagnosis of Human Fumarase Deficiency-Reference-Cited by-同舟云学术

Molecular Analysis and Prenatal Diagnosis of Human Fumarase Deficiency

Published:1998-04 Issue:4 Volume:63 Page:254-262
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Coughlin Eleanor M.,Christensen Ernst,Kunz Pamela L.,Krishnamoorthy K.S.,Walker Valerie,Dennis N.R.,Chalmers Ronald A.,Elpeleg Orly N.,Whelan Donald,Pollitt R.J.,Ramesh Vijaya,Mandell Roseann,Shih Vivian E.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference25 articles.

1. Intracellular distribution of fumarase in various animals;Akiba;J Biochem (Tokyo),1984

2. Rat liver mitochondrial and cytosolic fumarases with identical amino acid sequences are encoded from a single gene;Suzuki;J Biol Chem,1989

3. Nucleotide sequence of a cDNA coding for mitochondrial fumarase from human liver;Kinsella;Biosci Rep,1986

4. Presence of two forms of fumarase (fumarate hydratase E.C. 4.2.1.2) in mammalian cells: Immunological characterization and genetic analysis in somatic cell hybrids. Confirmation of the assignment of a gene necessary for the enzyme expression to human chromosome 1

5. Regional mapping of FH to band 1q42.1 by gene dosage studies;Despoisses;Cytogenet Cell Genet,1984

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