Toward a molecular understanding of ornithine transcarbamylase deficiency.

Advances in neurology ·Vol. 48 ·1988-00-00 ·Pages 71-81

Fox JE, Rosenberg LE

Abstract

暂无摘要

MeSH Terms

Chromosome Deletion DNA/genetics Female Genetic Carrier Screening Genetic Markers Humans Infant, Newborn Male Mitochondria, Liver/enzymology Ornithine Carbamoyltransferase/genetics Ornithine Carbamoyltransferase Deficiency Disease Pedigree Polymorphism, Restriction Fragment Length Prenatal Diagnosis X Chromosome/ultrastructure

Chemicals

Genetic Markers DNA Ornithine Carbamoyltransferase

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Fox J E

Schneider Children's Hospital, Long Island Jewish Medical Center, New Hyde Park, New York 11042.

Rosenberg L E

Article Info

Journal

Advances in neurology

Abbr.

Adv Neurol

ISSN

0091-3952

Published

1988-00-00

Pages

71-81

Language

English

Region

United States

NLM ID

0367524

Subset

External Links

PubMed source View journal details

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Toward a molecular understanding of ornithine transcarbamylase deficiency.

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