Whole exome sequencing reveals a homozygous SGCB variant in a Pakhtun family with limb girdle muscular dystrophy (LGMDR4) phenotype

Muhammad Tariq, Muhammad Latif, Memona Inam, Amin Jan, Nousheen Bibi, Hussein Sheikh Ali Mohamoud, Isse Ali, Habib Ahmad, Aziz Khan, Jamal Nasir, Abdul Wadood, Musharraf Jelani

Research output: Contribution to Journal › Article › peer-review

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Medicine & Life Sciences