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A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.

Nahum, S

A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp. [electronic resource] - Clinical and experimental dermatology Mar 2011 - 188-94 p. digital

Publication Type: Case Reports; Journal Article

ISSN: 1365-2230

Standard No.: 10.1111/j.1365-2230.2010.03944.x doi

Subjects--Topical Terms:
Adolescent
Amino Acid Substitution
DNA Mutational Analysis--methods
Female
Genotype
Humans
Hypotrichosis--genetics
Male
Microsatellite Repeats
Mutation, Missense
Pedigree
Receptors, Lysophosphatidic Acid--genetics
Scalp

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