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Phillipa Lamont

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American Journal of Human Genetics|August 24, 2004

Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1)Christopher Meredith, Ralf Herrmann, Cheryl Parry, et al.

American Journal of Human Genetics|November 27, 2010

Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with coresNyamkhishig Sambuughin, Kyle S Yau, Montse Olivé, et al.

Medrxiv : the Preprint Server for Health Sciences|February 26, 2024

Neuroradiological findings in GAA-<i>FGF14</i> ataxia (SCA27B): more than cerebellar atrophyShihan Chen, Catherine Ashton, Rawan Sakalla, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

American Journal of Human Genetics|August 24, 2004

Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1)Christopher Meredith, Ralf Herrmann, Cheryl Parry, et al.

American Journal of Human Genetics|November 27, 2010

Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with coresNyamkhishig Sambuughin, Kyle S Yau, Montse Olivé, et al.

Medrxiv : the Preprint Server for Health Sciences|February 26, 2024

Neuroradiological findings in GAA-<i>FGF14</i> ataxia (SCA27B): more than cerebellar atrophyShihan Chen, Catherine Ashton, Rawan Sakalla, et al.

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