Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss

Gorde:

Yoong, s.Y., ET AL., Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss. Archives of Disease in Childhood, Vol. 96, no. 9 (2011), p. 798-803.

Erref. 180932

Kokapena: SIIS R.186 Archivo

Zentroari eskatu

Hitz-gakoak:
Anomalías genéticas, Detección neonatal, Discapacidad auditiva, Estudio comparativo, Minorías, Reino Unido

Deskribapena
ISSN:	0003-9888 (papel) 1468-2044 (online)

Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss

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