R32W variant in Connexin 31: Mutation or polymorphism for deafness and skin disease? (multiple letters) [2]

N. López-Bigas, R. Rabionet, M. L. Arbonés, Xavier P. Estivill, D. Kelsell

Research output: Contribution to journalLetter

9 Citations (Scopus)
Original languageEnglish
Pages (from-to)70
Number of pages1
JournalEuropean Journal of Human Genetics
Volume9
Issue number1
Publication statusPublished - 2001
Externally publishedYes

Fingerprint

Connexins
Family Health
Deafness
Amino Acid Substitution
Skin Diseases
Mutation
human GJB3 protein

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

R32W variant in Connexin 31 : Mutation or polymorphism for deafness and skin disease? (multiple letters) [2]. / López-Bigas, N.; Rabionet, R.; Arbonés, M. L.; Estivill, Xavier P.; Kelsell, D.

In: European Journal of Human Genetics, Vol. 9, No. 1, 2001, p. 70.

Research output: Contribution to journalLetter

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AU - Kelsell, D.

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