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

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

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im November 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в листопаді 2018

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Bi-allelic Mutations in LSS, E ...... ecessive Hypotrichosis Simplex

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Bi-allelic Mutations in LSS, E ...... ecessive Hypotrichosis Simplex

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Bi-allelic Mutations in LSS, E ...... ecessive Hypotrichosis Simplex

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Bi-allelic Mutations in LSS, E ...... ecessive Hypotrichosis Simplex

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Bi-allelic Mutations in LSS, E ...... ecessive Hypotrichosis Simplex

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Bi-allelic Mutations in LSS, E ...... ecessive Hypotrichosis Simplex

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P1476

Bi-allelic Mutations in LSS, E ...... ecessive Hypotrichosis Simplex

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Alessandra Baumer

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Aylar Tafazzoli

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Dieter Lütjohann

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Dieter Metze

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Holger Thiele

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Janine Altmüller

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Jorge Frank

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Jürgen Ellwanger

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Maria-Teresa Romano

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Marta Bertolini

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P2860

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APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Potential role of nonstatin cholesterol lowering agents

Signal integration in the endoplasmic reticulum unfolded protein response

Lanosterol reverses protein aggregation in cataracts

Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris

Toxicologic lesions associated with two related inhibitors of oxidosqualene cyclase in the dog and mouse

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777-785

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scholarly article

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10.1016/J.AJHG.2018.09.011

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English

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103

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Peter Nürnberg

Ralf Paus

Alexander Rupp

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2018-11-01T00:00:00Z

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P698

30401459

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P921

Lanosterol synthase

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6218848

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