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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: Acta Neuropathol. 2020 Jan 3;139(3):565–582. doi: 10.1007/s00401-019-02117-6

Figure 1. Patients identified with a LGMD and POGLUT1 missense mutations.

Figure 1.

a Pedigrees of the nine independent families with different geographic origins (the family 1 has been reported elsewhere [35] and only the pedigree is included here); b patient II.1 from Family 2 with a congenital form showed scapular winging and elbow contractures (left), weakness and wasting of the biceps brachii (middle) and brachioradialis muscles (right).