M. Lovgren

A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies

Patricia E. Martin, M. Zamiri, A. Waters, 2020, Experimental dermatology.

Painful ulcers

D. Torley, A. G. Matthews, M. Lovgren, 2016, Clincal and Experimental Dermatology.

Update on skin directed therapies in mycosis fungoides.

J. Scarisbrick, M. Lovgren, 2019, Chinese clinical oncology.

Happle–Tinschert, Curry–Jones and segmental basal cell naevus syndromes, overlapping disorders caused by somatic mutations in hedgehog signalling genes: the mosaic hedgehog spectrum

S. Twigg, I. Colmenero, C. Moss, 2019, The British journal of dermatology.

Legal claims in Scottish National Health Service dermatology departments, 2002–2013

A. Drummond, M. Lovgren, L. McCrae, 2016, Clinical and experimental dermatology.

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening

C. Cole, A. Irvine, M. McAleer, 2017, The British journal of dermatology.