The phenotypic manifestations of hereditary tyrosinemia and tyrosyluria: a hypothesis.

Canadian Medical Association journal ·Vol. 97 ·No. 18 ·1967-10-28 ·Pages 1073-5

Scriver CR

Abstract

暂无摘要

MeSH Terms

Amino Acid Metabolism, Inborn Errors/genetics Humans Infant Tyrosine/blood,metabolism,urine

Chemicals

Tyrosine

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Scriver C R

References (1)

1 references, click to expand

[FANCONI'S SYNDROME WITH LIVER CIRRHOSIS IN AN INFANT].
Cesk Pediatr. 1963 Dec;18:1085-9 PMID: 14109667

Article Info

Journal

Canadian Medical Association journal

Abbr.

Can Med Assoc J

ISSN

0008-4409

Published

1967-10-28

Pages

1073-5

Language

English

Region

Canada

NLM ID

0414110

PMCID

PMC1923574

Subset

External Links

PubMed source PMC Full Text

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