Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR genein a patient with congenital bilateral absence of the vas deferens

Authors
Ravnik-Glavac, M Dean, M Glavac, D
Citation
M. Ravnik-glavac et al., Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR genein a patient with congenital bilateral absence of the vas deferens, HUMAN HERED, 50(5), 2000, pp. 318-319
Citations number
3
Categorie Soggetti
Molecular Biology & Genetics
Journal title
HUMAN HEREDITY
ISSN journal
00015652 → ACNP
Volume
50
Issue
5
Year of publication
2000
Pages
318 - 319
Database
ISI
SICI code
0001-5652(200009/10)50:5<318:TNMM(A>2.0.ZU;2-R