Tyrosinemie hereditaire de type I. A propos de trois observations
Revue Maghrebine de Pediatrie [La]. 1998; 8 (1): 35-43
in French
| IMEMR
| ID: emr-49512
Subject(s)
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Rickets
/
Amino Acid Metabolism, Inborn Errors
/
Genetic Diseases, Inborn
/
Liver Cirrhosis
Type of study:
Case report
Limits:
Female
/
Humans
/
Male
Language:
French
Journal:
Rev. Maghreb. Pediatr.
Year:
1998
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