Inam, Memona
3  Ergebnisse:
Personensuche X
?
2

Whole exome sequencing reveals a homozygous SGCB variant in..:

Tariq, Muhammad ; Latif, Muhammad ; Inam, Memona...
http://nectar.northampton.ac.uk/15701/1/2020_Tariq_Muhammad_etal_Elsevier_Whole_exome_sequencing_reveals_a_homozygous_SGCB_variant_in_a_Pakhtun_family_with_limb_girdle_muscular_dystrophy_LGMDR4_phenotype.pdf.  , 2021
 
?
3

Whole exome sequencing reveals a homozygous SGCB variant in..:

Tariq, Muhammad ; Latif, Muhammad ; Inam, Memona...
Tariq , M , Latif , M , Inam , M , Jan , A , Bibi , N , Mohamoud , H S A , Ali , I , Ahmad , H , Khan , A , Nasir , J , Wadood , A & Jelani , M 2021 , ' Whole exome sequencing reveals a homozygous SGCB variant in a Pakhtun family with limb girdle muscular dystrophy (LGMDR4) phenotype ' , Gene Reports , vol. 22 , 101014 . https://doi.org/10.1016/j.genrep.2020.101014.  , 2021
 
1-3