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Article

A novel mutation in SLURP1 in patients with mal de Meleda from the Indian subcontinent.

Journal of dermatological science - 1 Oct 2015

Nellen Ruud G L, Claessens Tijs, Subramaniam Ranugha, Betkerur Jayadev, Prashanth Akila, Steijlen Peter M, van Geel Michel

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Source

Identifiers

PMID: 26254200
DOI: 10.1016/j.jdermsci.2015.07.013

Genes

SLURP1

Provenance

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel mutation in SLURP1 in patients with mal de Meleda from the Indian subcontinent.PMID 26254200Read ↗

A novel mutation in SLURP1 in patients with Mal de Meleda from Turkey.Semantic proximity Read ↗

A novel homozygous missense mutation in SLURP1 causing Mal de Meleda with an atypical phenotype.Semantic proximity Read ↗

A Japanese case of Mal de Meleda with SLURP1 mutation.Semantic proximity Read ↗

Identification of a novel compound heterozygous mutation and a homozygous mutation of SLURP1 in Chinese families with Mal de Meleda.Semantic proximity Read ↗

Mutations in the gene encoding SLURP-1 in Mal de Meleda.Semantic proximity Read ↗

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates.Semantic proximity Read ↗

Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda.Semantic proximity Read ↗

Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous.Semantic proximity Read ↗

A novel mutation in the ARS (component B) gene encoding SLURP-1 in a family with Mal de Meleda.Semantic proximity Read ↗

Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma.Semantic proximity Read ↗

A novel missense mutation in the gene encoding SLURP-1 in patients with Mal de Meleda from northern Tunisia.Semantic proximity Read ↗

Identification of recurrent mutations in the ARS (component B) gene encoding SLURP-1 in two families with mal de Meleda.Semantic proximity Read ↗

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