Familial study of spinal muscular atrophy carriers with SMN1 (2+0) genotype.

Yanyan, Cao; Miaomiao, Cheng; Fang, Song; Yujin, Qu; Jinli, Bai; Hong, Wang

Yanyan, Cao; Miaomiao, Cheng; Fang, Song; Yujin, Qu; Jinli, Bai; Hong, Wang.

Affiliation

Yanyan C; Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.
Miaomiao C; Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.
Fang S; Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.
Yujin Q; Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.
Jinli B; Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.
Hong W; Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.

Yi Chuan ; 43(2): 160-168, 2021 Feb 16.

Article de En | MEDLINE | ID: mdl-33724218

Sujet(s)
Mots clés

(2+0) genotype; SMN1; STR linkage analysis; polymorphism; spinal muscular atrophy

Texte intégral

Ajouter à My VHL

Imprimer

XML

PubMed Links

Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Amyotrophie spinale Limites: Child / Humans Langue: En Journal: Yi Chuan Sujet du journal: GENETICA Année: 2021 Type de document: Article Pays d'affiliation: Chine Pays de publication: Chine

Texte intégral

Ajouter à My VHL

Imprimer

XML

PubMed Links

Recherche sur Google