The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada
about
Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from IndiaMutational analyses of Tay-Sachs disease: studies on Tay-Sachs carriers of French Canadian background living in New England.Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic areaHeterozygosity for Tay-Sachs disease in non-Jewish Americans with ancestry from Ireland or Great Britain.Selection in the Ashkenazi Jewish Population Unlikely—Reply to Zlotogora and Bach.Geographic distribution of 18 autosomal recessive disorders in the French Canadian population of Saguenay-Lac-Saint-Jean, Quebec
P2860
The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada
description
1992 nî lūn-bûn
@nan
1992 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
The intron 7 donor splice site ...... ease mutation in French Canada
@ast
The intron 7 donor splice site ...... ease mutation in French Canada
@en
The intron 7 donor splice site ...... ease mutation in French Canada
@nl
type
label
The intron 7 donor splice site ...... ease mutation in French Canada
@ast
The intron 7 donor splice site ...... ease mutation in French Canada
@en
The intron 7 donor splice site ...... ease mutation in French Canada
@nl
prefLabel
The intron 7 donor splice site ...... ease mutation in French Canada
@ast
The intron 7 donor splice site ...... ease mutation in French Canada
@en
The intron 7 donor splice site ...... ease mutation in French Canada
@nl
P2093
P356
P1433
P1476
The intron 7 donor splice site ...... ease mutation in French Canada
@en
P2093
E Andermann
J Larochelle
M De Braekeleer
P Hechtman
S Melançon
P2888
P356
10.1007/BF00220467
P407
P577
1992-12-01T00:00:00Z
P6179
1013691201