论文信息 - Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant - 字舞流文

Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant

M. Skopkova | D. Gašperíková | P. Seeman | L. Varga | Zuzana Slobodova | A. Ficek | J. Laštůvková | D. Šafka Brožková | A. Soltysova | J. Jenčík | Anna Uhrová Mészárosová