Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex - Concepedia

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Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex

DOI Full Paper Access

76

Citations

25

References

2018

Year

M. T. Romano, Aylar Tafazzoli, Maximilian Mattern, Sugirthan Sivalingam, Sabrina Wolf, Alexander Rupp, Hölger Thiele, Janine Altmüller, Peter Nürnberg, Jürgen Ellwanger,

The American Journal of Human Genetics

Bi-allelic MutationsAllelic VariantMendelian DisorderEncoding Lanosterol SynthaseGenetic DisorderGeneticsInherited Metabolic DiseasePathologyMolecular GeneticsGene ExpressionMedicine

References

	Year	Citations

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