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La Revue du praticien - 15 Jan 1997
Vidaud M
Identification of mutations responsible for human monogenic hereditary diseases has lately undergone rapid development. It is now possible to establish the mutation spectrum for a given genetic disease and international databases are now available on the Internet. New mutational mechanisms have b...
PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9157512-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.
Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.
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