Whole exome sequencing reveals a homozygous SGCB variant in a Pakhtun family with limb girdle muscular dystrophy (LGMDR4) phenotype
Titel:
Whole exome sequencing reveals a homozygous SGCB variant in a Pakhtun family with limb girdle muscular dystrophy (LGMDR4) phenotype
Auteur:
Tariq, Muhammad Latif, Muhammad Inam, Memona Jan, Amin Bibi, Nousheen Mohamoud, Hussein Sheikh Ali Ali, Isse Ahmad, Habib Khan, Aziz Nasir, Jamal Wadood, Abdul Jelani, Musharraf