Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients

  1. Álvarez, A.
  2. Del Castillo, I.
  3. Pera, A.
  4. Villamar, M.
  5. Moreno-Pelayo, M.A.
  6. Rivera, T.
  7. Solanellas, J.
  8. Moreno, F.
Aldizkaria:
Journal of Medical Genetics

ISSN: 0022-2593

Argitalpen urtea: 2003

Alea: 40

Zenbakia: 8

Orrialdeak: 636-639

Mota: Artikulua

DOI: 10.1136/JMG.40.8.636 GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus