Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Bahareh Hasani‐sabzevar"'
Autor:
Najmeh Ahangari, Nazanin Gholampour‐Faroji, Mohammad Doosti, Majid Ghayour Mobarhan, Sima Shahrokhzadeh, Ehsan Ghayoor Karimiani, Bahareh Hasani‐sabzevar, Paria Najarzadeh Torbati, Aliakbar Haddad‐Mashadrizeh
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Background ECEL1 has been presented as a causal gene of an autosomal recessive form distal arthrogryposis (DA) which affects the distal joints. The present study focused on bioinformatic analysis of a novel mutation in ECEL1, c.535A>G (p. Ly
Externí odkaz:
https://doaj.org/article/91023b0d55f247c3ac3004b077a41807
Autor:
Mohammad Doosti, Aliakbar Haddad-Mashadrizeh, Paria Najarzadeh Torbati, Nazanin Gholampour-Faroji, Ehsan Ghayoor Karimiani, Najmeh Ahangari, Bahareh Hasani sabzevar, Sima Shahrokhzadeh, Majid Ghayour Mobarhan
Background: ECEL1 has been represented as a causal gene of an autosomal recessive form distal arthrogryposis (DA) which affects the distal joints. The present study focused on bioinformatic analysis of a novel mutation in ECEL1, c.535A>G (p. Lys179Gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f414c38d2e4aa1efe722748352679180
https://doi.org/10.22541/au.160518606.62434555/v1
https://doi.org/10.22541/au.160518606.62434555/v1
