Phenylketonuria: a clinical and genetic study of British families
dc.contributor.author
Munro, Thomas A.
en
dc.date.accessioned
2019-02-15T14:38:22Z
dc.date.available
2019-02-15T14:38:22Z
dc.date.issued
1940
dc.description.abstract
This thesis analyses 43 families with 86 cases of phenylketonuria,
a rare metabolic disorder always associated with mental defect and
occurring in about 4 per 100,000 persons, defines the symptomatology,
discusses the pathology and biochemistry, proves the inheritance
of the disease as a Mendelian recessive Character, records the presence
of other mental disorders in the families and reviews the literature.
en
dc.identifier.uri
http://hdl.handle.net/1842/35434
dc.publisher
The University of Edinburgh
en
dc.relation.ispartof
Annexe Thesis Digitisation Project 2019 Block 22
en
dc.relation.isreferencedby
en
dc.title
Phenylketonuria: a clinical and genetic study of British families
en
dc.type
Thesis or Dissertation
en
dc.type.qualificationlevel
Doctoral
en
dc.type.qualificationname
MD Doctor of Medicine
en
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