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Article

Phenylalanine hydroxylase deficiency in a population in Germany: mutational profile and nine novel mutations.

Human mutation - 1 Jan 1996

Guldberg P, Mallmann R, Henriksen K F, Güttler F

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Identifiers

PMID: 8889590
DOI: 10.1002/(SICI)1098-1004(1996)8:3<276::AID-HUMU14>3.0.CO;2-#

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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