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Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin gene. [electronic resource] by
- Leshinsky-Silver, E
- Argov, Z
- Rozenboim, L
- Cohen, S
- Tzofi, Z
- Cohen, Y
- Wirguin, Y
- Dabby, R
- Lev, D
- Sadeh, M
Producer: 20080307
In:
Neuromuscular disorders : NMD vol. 17
Availability: No items available.
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13.
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Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency. [electronic resource] by
- Leshinsky-Silver, E
- Levine, A
- Nissenkorn, A
- Barash, V
- Perach, M
- Buzhaker, E
- Shahmurov, M
- Polak-Charcon, S
- Lev, D
- Lerman-Sagie, T
Producer: 20040601
In:
Molecular genetics and metabolism vol. 79
Availability: No items available.
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14.
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NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement. [electronic resource] by
- Leshinsky-Silver, E
- Lebre, Anne-Sophie
- Minai, Limor
- Saada, Ann
- Steffann, Julie
- Cohen, Sarit
- Rötig, Agnes
- Munnich, Arnold
- Lev, Dorit
- Lerman-Sagie, Tally
Producer: 20090812
In:
Molecular genetics and metabolism vol. 97
Availability: No items available.
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CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine. [electronic resource] by
- Stam, A H
- Vanmolkot, K R J
- Kremer, H P H
- Gärtner, J
- Brown, J
- Leshinsky-Silver, E
- Gilad, R
- Kors, E E
- Frankhuizen, W S
- Ginjaar, H B
- Haan, J
- Frants, R R
- Ferrari, M D
- van den Maagdenberg, A M J M
- Terwindt, G M
Producer: 20081215
In:
Clinical genetics vol. 74
Availability: No items available.
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