Accès libre

A novel c.973G>T mutation in the ε-subunit of the acetylcholine receptor causing congenital myasthenic syndrome in an iranian family

, ,  et   
28 août 2019
À propos de cet article

Citez
Télécharger la couverture

Figure 1

The photographs of the patient with bilateral ptosis (here he is 2 and a half years old).
The photographs of the patient with bilateral ptosis (here he is 2 and a half years old).

Figure 2

(a) Pedigree of the family, electropherogram of sequences from exon 12 of CHRNE, (b) carrier parents; the case illustrating the c.973G>T of the CHRNE gene mutation.
(a) Pedigree of the family, electropherogram of sequences from exon 12 of CHRNE, (b) carrier parents; the case illustrating the c.973G>T of the CHRNE gene mutation.
Langue:
Anglais
Périodicité:
2 fois par an
Sujets de la revue:
Médecine, Sciences médicales de base, Sciences médicales de base, autres